CN100345830C - Condensed heteroaryl derivatives - Google Patents
Condensed heteroaryl derivatives Download PDFInfo
- Publication number
- CN100345830C CN100345830C CNB2004100557609A CN200410055760A CN100345830C CN 100345830 C CN100345830 C CN 100345830C CN B2004100557609 A CNB2004100557609 A CN B2004100557609A CN 200410055760 A CN200410055760 A CN 200410055760A CN 100345830 C CN100345830 C CN 100345830C
- Authority
- CN
- China
- Prior art keywords
- group
- alkyl
- alkylidene group
- milligrams
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Medicinal compositions which are useful as phosphatidylinositol 3-kinase (PI3K) inhibitors and anticancer agents; and novel bicyclic or tricyclic condensed heteroaryl derivatives or salts thereof having favorable effects of inhibiting PI3K and suppressing the proliferation of cancer cells.
Description
The application is that international application no is PCT/JP 01/03650, and international filing date is national applications the dividing an application for the Chinese patent application of " condensed heteroaryl derivatives " that number be 01808654.3 title after the PCT international application in April 26 calendar year 2001 enters China's stage.
Technical field
The present invention relates to condensed heteroaryl derivatives as medicine, particularly phosphatidyl-inositol 3-kinase (PI3K) inhibitor and carcinostatic agent.
Background technology
Phosphatidylinositols (hereinafter referred to as " PI ") is one of cell membrane phospholipid, known it play a part the cell internal information and transmit.Recognize well that particularly (PI (4 for PI (4,5) bisphosphate; 5) P2) resolve into DG and inositol (1,4,5) triphosphoric acid because of Phospholipase C; the activation and the intracellular Ca2+ that cause protein kinase C are mobilized [MJBerridge etc., Nature (nature), 312; 315; (1984), Y Nishizuka, Science (science); 225,1365 (1984)].
On the other hand, latter half in the 1980's, identified PI3K be the enzyme that makes 3 phosphorylations of PI class inositol ring [D Whitman etc., Nature, 332,664 (1988)].
PI3K once was considered to single enzyme when finding originally.In recent years, determined that there is hypotype in PI3K, be divided into following 3 classes [B Vanhaesebroeck, Trend in Biol.Sci., 22,267 (1997)] by external substrate specificity.
The I fermentoid is a substrate with PI, PI (4) P, PI (4,5) P2, but best substrate is PI (4,5) P2 in cell.The I fermentoid is divided into two classes (Ia class, Ib class) again according to activating mechanism.The Ia class is activated by the tyrosine-kinase enzyme system, comprises p110 α, p110 β and p110 δ hypotype.The Ib class comprises by the p110 γ hypotype of the receptor activation of G albumen coupling.
The II fermentoid is with PI, and PI (4) P is a substrate, but is not substrate with PI (4,5) P2.This kind of enzyme comprises PI3K C2 α, C2 β and C2 γ hypotype, it is characterized in that C-terminal has the C2 zone, and this illustrates that they are active by calcium ion control.The III fermentoid is a substrate with PI only.It is unclear that the activating mechanism of this kind of enzyme.Each hypotype all has active regulation mechanism itself, thinks that therefore they can respond inherent and stimulate and activate.
What research was carried out at most in the PI3K hypotype is the Ia hypotype.The hypotype of Ia class is to be made of the regulator subunit of the catalytic subunit of 110kDa (subunit) and 85/55kDa.Regulator subunit contains the SH2 structural domain, can be combined by the tyrosine residues with growth factor receptors with tyrosine kinase activity or oncoprotein phosphorylation.As a result, caused the PI3K activity of p110 catalytic subunit.Therefore, think that Ia hypotype and cell proliferation are carcinogenic relevant.In addition, Ia class PI3K and active form ras combination show enzymic activity, have determined that active form ras is present in the multiple cancer, and this illustrates that Ia class PI3K is relevant with the canceration of cell.
As mentioned above, expection PI3K inhibitor can be used as the novel medicine that is used for cell proliferation disorders, particularly carcinostatic agent.As the PI3K inhibitor, known have a wortmannin[H Yano etc., J Biol Chem., 263,16178,1993] and the represented LY294002[CJ Vlahos of following formula etc., J Biol Chem., 269,5241,1994], but urgent wish to develop to have the inhibiting PI3K inhibitor of stronger cancer cell multiplication.
In the Te Kaiping 6-220059 communique, disclosed the represented condensed heteroaryl derivatives of following formula (a) with hypoglycemic activity.In addition, Indian J.Chem. is arranged respectively, Sect.B (1993), 32B (9), 965-8 have disclosed the represented compound of following formula (b), J.Heterocycl.Chem. (1992), 29 (7), 1693-702 has disclosed the synthetic method of the represented compound of following formula (c), also has Al-Azharbull.Sci. (1992), 3 (2), 767-75 has disclosed the represented compound with anti-microbial activity of following formula (d).But these existing documents had not both disclosed yet not explanation for the PI3K restraining effect.
(in (a) formula, Z represents O, S or N-R
0, R
1Expression can have substituent amino maybe can have substituent heterocyclic radical etc., R
2Expression cyano group, can have substituent amino and maybe can have substituent heterocyclic radical.Other definition is with reference to this communique.(b) and (c) in the formula, R represents (replacement) amino or (replacement) nitrogenous saturated heterocyclyl.)
In the WO98/23613 communique, disclosed as fused pyrimidine derivative with tyrosine kinase receptor inhibiting carcinostatic agent etc., as the amino that has on 4 specific heteroaryl to replace, amino that phenyl replaces or 1-indyl, 2 go up unsubstituted 7H-pyrrolo-[2,3-d] pyrimidine derivatives.
In addition, the represented A of aftermentioned general formula (I) ring for as (b) compound of represented ring is as follows,
(1) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidine also, it as have anti-inflammatory, spasmolysis (antiinflammatory, compound spasmolytic) is set forth in Ann.Pharm, Fr. (1974), 32 (11), 575-9,
(2) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidines-7 (1H)-ketone also, it is set forth in Chem.Pharm.Bull. (1976) as the compound with diuretic properties (diuretic activity), and 24 (9), 2057-77,
(3) 4-(4-the morpholinyl)-pure and mild 6-methoxyl group-4-of 2-phenyl-6-quinazoline (4-morpholinyl)-2-phenylquinazoline, it is as the compound with anti-microbial activity (antibiotic), be set forth in Khim.Farm.Zh. (1993), 7 (7), 16-19 and Khim.Geterotsiki.Soedin. (1971), 7 (3), 418-20
(4) 2,4-diamino-6-phenyl-8-piperidines is for Mi Dingbing [5,4-d] pyrimidine, and it is set forth in the WO2000/41697 communique as the compound with cerebral ischemia prophylactic treatment effect (celebral ischemia),
(5) B is that phenyl ring, W are that N, n are 2 or 3, the R that exists in the aftermentioned general formula (Ib)
1All be-OMe and R
4bFor not replacing or be selected from the compound of the phenyl of 1～3 following substituting group replacement :-halogen ,-NO
2,-low alkyl group ,-the O-low alkyl group ,-junior alkyl halides and-CONRaRc, it is set forth in WO99/32460 as cardiovascular disease medicine (cardiovascular),
(6) B is that phenyl ring, W are that N, n are 1, R in the aftermentioned general formula (Ib)
1For-halogen or-low alkyl group and R
4bFor-compound of (can have substituent imidazolyl), it is set forth in No. 841669 communiques of BE as antiparasitic (antiparasitics),
(7) B is that thiphene ring and W are the compound of CH in the aftermentioned general formula (Ib), and it is set forth in the WO99/43682 communique as anxiolytic (antianxiety),
(8) B is that imidazole ring and W are the compound of N in the aftermentioned general formula (Ib), and it has antiinflammation and platelet aggregation restraining effect etc., be set forth in the spy and open clear 62-10085 communique and 61-158983 communique,
(9) B is pyridine ring and R in the aftermentioned general formula (Ib)
4bFor unsubstituted phenyl, unsubstituted pyridine base or-compound of low-grade alkylidene-(can have substituent nitrogenous saturated heterocyclyl), it has spasmolysis, diuretic properties (spasmolytic, diuretic) or hypotensive activity (hypotensive activity), be set forth in US3873545 communique and Act Pol.Pharm. (1994), 51 (4-5), 359-63
(10) B is pyrazine ring and R in the aftermentioned general formula (Ib)
4bBe the compound of unsubstituted phenyl or benzyl, it has vasodilation and sedative effect (coronary dilating, sedative acitivity), is set forth in the US2940972 communique,
(11) B is phenyl ring and R in the aftermentioned general formula (Ib)
4bBe the compound of styryl or 2-(5-nitro-2-furyl) vinyl, it has antiinflammation or anti-microbial activity, is set forth in No. 2140280 communique of No. 3753981 communiques of US and German Patent, and
(12) B is that phenyl ring, W are CH and R in the aftermentioned general formula (Ib)
2And R
3Become with adjacency-the N atom links to each other-(can have substituent piperidyl) or-compound of (can have substituent piperazinyl), respectively in Eur.J.Med.Chem. (1996), 31 (5), among the 417-425, as benzene phenodiazine receptors ligand (benzodiazepine receptor ligand), in No. 4560692 communiques of US, as compound with spasmolysis and stable effect etc., also open in the flat 2-129169 communique, as compound with lipid peroxidation restraining effect etc. the spy.
In addition, B is that pyridine ring and n are 0 compound in the aftermentioned general formula (Ib), be disclosed in following document: the spy opens flat 51-138689 communique (antiparasitic), Te Kaiping 56-120768 communique (colour component of thermal recording medium), Antimicrob.Agents Chemother., (1975), 8 (2), 216-19 (anti-microbial effect), Cancer Res. (1975), 35 (12), 3611-17 (mutagenesis), CA64:19608c, Collect.Czech.Chem.Commun., (1994), 59 (6), 1463-6, No. 5304554 communique of United States Patent (USP) (anti-HIV (hiv virus) effect), Chem.Pharm.Bull., (1982), 30 (6), 1974-9, and J.Heterocycl.Chem. (1980), 17 (5), 1029-34.But, in these existing documents PI3K restraining effect and antitumous effect had not both been disclosed yet not explanation.
Summary of the invention
The present inventor has furtherd investigate has inhibiting compound to PI3K, finds that novel condensed heteroaryl derivatives has good PI3K restraining effect and cancer cell multiplication restraining effect, can become good PI3K inhibitor and carcinostatic agent, thereby finish the present invention.
Therefore, the present invention relates to the medical composition as PI3K inhibitor or carcinostatic agent, it comprises and shows down the carrier that allows on condensed heteroaryl derivatives that general formula (I) is represented or its salt and the pharmacopedics.
(mark in the formula is represented following implication
B: phenyl ring or contain the heteroatomic 5-6 of 1～2 of being selected from O, S and N unit monocycle hetero-aromatic ring,
R
1:-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-cycloalkyl ,-can have substituent aryl, can have substituent heteroaryl ,-halogen ,-NO
2,-CN ,-junior alkyl halides ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb or-NRaCO-COORb ,-the nitrogenous saturated heterocyclic of CO-,-CONRa-low-grade alkylidene-ORb ,-CONRa-low-grade alkylidene-NRbRc ,-O-low-grade alkylidene-ORb ,-O-low-grade alkylidene-O-low-grade alkylidene-ORb ,-O-low-grade alkylidene-NRaRb ,-O-low-grade alkylidene-O-low-grade alkylidene-NRaRb ,-O-low-grade alkylidene-NRc-low-grade alkylidene-NRaRb ,-NRc-low-grade alkylidene-NRaRb ,-N (low-grade alkylidene-NRaRb)
2,-CONRa-ORb ,-NRa-CO-NRbRc or-OCORb,
R
2And R
3: can be identical also can be different, for-H ,-low alkyl group ,-low-grade alkylidene-ORa or-low-grade alkylidene-NRaRc, perhaps R
2And R
3With the N atom of adjacency be connected to can have substituent nitrogenous saturated heterocyclyl promptly-NR
2R
3,
Ra and Rc: can be identical also can be different, for-H or-low alkyl group,
Rb: for-H ,-low alkyl group, cycloalkyl, can have substituent aryl and maybe can have substituent heteroaryl,
N:0,1,2 or 3,
W and X: can be identical also can be different, be N or CH,
Y:O, S or NH,
R
4: for-H,-low alkyl group,-low-grade alkenyl,-low-grade alkynyl,-(can have substituent aryl),-low-grade alkylidene-(can have substituent aryl),-lower alkenylene-(can have substituent aryl),-rudimentary alkynylene-(can have substituent aryl),-(can have substituent cycloalkyl),-(can have substituent cycloalkenyl group),-low-grade alkylidene-(can have substituent cycloalkyl),-lower alkenylene-(can have substituent cycloalkyl),-low-grade alkylidene-(can have substituent nitrogenous saturated heterocyclyl),-lower alkenylene-(can have substituent nitrogenous saturated heterocyclyl),-(can have substituent heteroaryl),-low-grade alkylidene-(can have substituent heteroaryl) or-lower alkenylene-(can have substituent heteroaryl).Below identical.)
The compounds of this invention (I) comprises the commercial compound of putting down in writing in the known compound put down in writing in the contained aforementioned background art of this definition and the aftermentioned embodiment table such as compound Z.
The invention still further relates to general formula (Ia) or (Ib) represented novel condensed heteroaryl derivatives or its salt, and the novel pharmaceutical composition that comprises the carrier that allows on this compound or its salt and the pharmacopedics.
(mark in the formula is represented following implication
R
1:-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-cycloalkyl ,-can have substituent aryl, can have substituent heteroaryl ,-halogen ,-NO
2,-CN ,-junior alkyl halides ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb or-NRaCO-COORb ,-the nitrogenous saturated heterocyclic of CO-,-CONRa-low-grade alkylidene-ORb ,-CONRa-low-grade alkylidene-NRbRc ,-O-low-grade alkylidene-ORb ,-O-low-grade alkylidene-O-low-grade alkylidene-ORb ,-O-low-grade alkylidene-NRaRb ,-O-low-grade alkylidene-O-low-grade alkylidene-NRaRb ,-O-low-grade alkylidene-NRc-low-grade alkylidene-NRaRb ,-NRc-low-grade alkylidene-NRaRb ,-N (low-grade alkylidene-NRaRb)
2,-CONRa-ORb ,-NRa-CO-NRbRc or-OCORb,
R
2With RU: can be identical also can be different, for-H or-low alkyl group, perhaps R
2And R
3With the N atom of adjacency be connected to can have substituent nitrogenous saturated heterocyclyl promptly-NR
2R
3,
Ra and Rc: can be identical also can be different, for-H or-low alkyl group,
Rb: for-H ,-low alkyl group, cycloalkyl, can have substituent aryl and maybe can have substituent heteroaryl,
N:0,1,2 or 3,
X:N or CH,
Y:O, S or NH,
R
4a: for-(can have substituent aryl),-low-grade alkylidene-(can have substituent aryl),-lower alkenylene-(can have substituent aryl),-rudimentary alkynylene-(can have substituent aryl),-(can have substituent cycloalkyl),-(can have substituent cycloalkenyl group),-low-grade alkylidene-(can have substituent cycloalkyl),-lower alkenylene-(can have substituent cycloalkyl),-low-grade alkylidene-(can have substituent nitrogenous saturated heterocyclyl),-lower alkenylene-(can have substituent nitrogenous saturated heterocyclyl),-(can have substituent heteroaryl),-low-grade alkylidene-(can have substituent heteroaryl) or-lower alkenylene-(can have substituent heteroaryl).
But except the following compound,
(1) X is that N, Y are that S, n are 3, R
1For-CN ,-combination and the R of OEt (oxygen ethyl) and phenyl
4aBe the compound of 2-nitrophenyl,
(2) X is CH and R
4aFor-compound of (can have substituent heteroaryl),
(3) X is that CH, Y are that O, n are 0 and R
4aBe the compound of unsubstituted phenyl, and
(4) X is that N, Y are that S, n are 2, R
1All be unsubstituted phenyl and R
4aCompound for 4-p-methoxy-phenyl or unsubstituted phenyl.Below identical.)
(mark in the formula is represented following implication
B: phenyl ring or contain the heteroatomic 5-6 of 1～2 of being selected from O, S and N unit monocycle hetero-aromatic ring,
R
1:-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-cycloalkyl ,-can have substituent aryl, can have substituent heteroaryl ,-halogen ,-NO
2,-CN ,-junior alkyl halides ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb ,-NRaCO-COORb ,-NRaCOORb ,-NRaCO-low-grade alkylidene-aryl ,-NRa-SO
2-low-grade alkylidene-aryl,-NRa-low-grade alkylidene-aryl,-low-grade alkylidene-ORb,-low-grade alkylidene-NRaRb, the nitrogenous saturated heterocyclic of-CO-,-CONRa-low-grade alkylidene-ORb,-CONRa-low-grade alkylidene-NRcRb,-CONRa-low-grade alkylidene-nitrogenous saturated heterocyclic,-O-low-grade alkylidene-ORb,-O-low-grade alkylidene-NRaRb,-O-low-grade alkylidene-nitrogenous saturated heterocyclic,-O-low-grade alkylidene-O-low-grade alkylidene-ORb,-O-low-grade alkylidene-O-low-grade alkylidene-NRaRb,-O-low-grade alkylidene-NRc-low-grade alkylidene-NRaRb,-NRc-low-grade alkylidene-NRaRb,-N (low-grade alkylidene-NRaRb)
2,-CONRa-ORb ,-NRa-CO-NRbRc or-OCORb,
R
2And R
3: with the N atom of adjacency be connected to can have substituent nitrogenous saturated heterocyclyl promptly-NR
2R
3,
Ra and Rc: can be identical also can be different, for-H or-low alkyl group,
Rb: for-H ,-low alkyl group, cycloalkyl, can have substituent aryl and maybe can have substituent heteroaryl,
N:0,1,2 or 3, but n is 1,2 or 3 when B is phenyl ring,
W: be N or CH,
R
4b: for-(can have substituent aryl),-low-grade alkylidene-(can have substituent aryl),-lower alkenylene-(can have substituent aryl),-rudimentary alkynylene-(can have substituent aryl),-(can have substituent cycloalkyl),-(can have substituent cycloalkenyl group),-low-grade alkylidene-(can have substituent cycloalkyl),-lower alkenylene-(can have substituent cycloalkyl),-low-grade alkylidene-(can have substituent nitrogenous saturated heterocyclyl),-lower alkenylene-(can have substituent nitrogenous saturated heterocyclyl),-(can have substituent heteroaryl),-low-grade alkylidene-(can have substituent heteroaryl) or-lower alkenylene-(can have substituent heteroaryl).
But except the following compound,
(1) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidine also,
(2) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidines-7 (1H)-ketone also,
(3) 4-(4-the morpholinyl)-pure and mild 6-methoxyl group-4-of 2-phenyl-6-quinazoline (4-morpholinyl)-2-phenylquinazoline,
(4) 2,4-diamino-6-phenyl-8-piperidines is for Mi Dingbing [5,4-d] pyrimidine,
(5) B is that phenyl ring, W are the R that N, n are 2 or 3, exist
1All be-OMe (oxygen methyl) and R
4bFor not replacing or be selected from the compound of the phenyl of 1～3 following substituting group replacement :-halogen ,-NO
2,-low alkyl group ,-the O-low alkyl group ,-junior alkyl halides and-CONRaRc,
(6) B is that phenyl ring, W are that N, n are 1, R
1For-halogen or-low alkyl group and R
4bFor-compound of (can have substituent imidazolyl),
(7) B is that thiphene ring and W are the compound of CH,
(8) B is that imidazole ring and W are the compound of N,
(9) B is pyridine ring and R
4bFor unsubstituted phenyl, unsubstituted pyridine base or-compound of low-grade alkylidene-(can have substituent nitrogenous saturated heterocyclyl),
(10) B is pyrazine ring and R
4bBe the compound of unsubstituted phenyl or benzyl,
(11) B is phenyl ring and R
4bBe the compound of styryl or 2-(5-nitro-2-furyl) vinyl, and
(12) B is that phenyl ring, W are CH and R
2And R
3Be link to each other with the N atom of adjacency become-(can have substituent piperidyl) or-compound of (can have substituent piperazinyl).Below identical.)
In addition, the present invention also provides the methods of treatment with PI3K diseases associated (particularly cancer), it comprises to the human or animal takes the general formula (I), (Ia) of significant quantity or (Ib) represented condensed heteroaryl derivatives or its salt, and this condensed heteroaryl derivatives or its salt purposes in the medicine for treatment thing made from the PI3K diseases associated (particularly carcinostatic agent) also is provided.
The preferred forms of invention
Further specify general formula (I), (Ia) and compound (Ib) below.
In this specification sheets, term " rudimentary " is meant that carbonatoms is 1～10, preferred 1～6, more preferably 1～3 straight or branched hydrocarbon chain.
As " low alkyl group ", preferably carbonatoms is 1～6 a alkyl, especially preferably methyl and ethyl.As " low-grade alkenyl ", preferably vinyl, allyl group, 1-propenyl, pseudoallyl, 1-butylene base, crotyl and 3-butenyl etc.As " low-grade alkynyl ", preferably ethynyl, 1-proyl, 2-propynyl, ethyl acetylene base, 2-butyne base, 3-butynyl, 1-methyl-2-propynyl etc.As " low-grade alkylidene ", " lower alkenylene " and " rudimentary alkynylene ", be the divalent radical of aforementioned low alkyl group, low-grade alkenyl and low-grade alkynyl, preferably methylene radical, ethylidene, vinylidene, propenylidene, ethynylene and inferior proyl.As " cycloalkyl " and " cycloalkenyl group ", preferably carbonatoms is 3～8 cycloalkyl and cycloalkenyl group, especially preferably cyclopropyl, cyclopentyl, cyclohexyl and cyclopentenyl.
As " halogen ", what can exemplify has F, Cl, Br and an I atom.As " junior alkyl halides ", be the aforementioned low alkyl group that can be replaced by more than one aforementioned halogen atom, preferably-CF
3
In this specification sheets, " nitrogenous saturated heterocyclyl " be annular atoms comprise 1～2 N atom, also can contain the annular atoms of 1 O or S atom, also can have the nitrogenous saturated heterocyclyl of 5-7 unit of bridging, can condense with phenyl ring.Preferably pyrrolidyl, piperazinyl, piperidyl and morpholinyl.In addition ,-NR
2R
3The nitrogenous saturated heterocyclyl that forms, preferably 1-pyrrolidyl, 1-piperazinyl, piperidino-(1-position only) and morpholino, especially preferably morpholino.
In this specification sheets, term " aryl " is meant aromatic cyclic hydrocarbon group, and preferably carbonatoms is 6～14 a aryl, is more preferably phenyl and naphthyl.
In this specification sheets, " heteroaryl " be meant contain 1-4 be selected from N, S, O heteroatomic 5-6 unit's bicyclic heteroaryl and and phenyl ring condense the 2 ring type heteroaryls that form, it can be a fractional saturation.Here, as bicyclic heteroaryl, preferably furyl, thienyl, pyrryl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, azoles base, different azoles base, triazolyl, tetrazyl, thiadiazolyl group, pyridyl, pyrimidyl, pyridazinyl, pyrazinyl; As 2 ring type heteroaryls, preferably benzofuryl, benzothienyl, diazosulfide base, benzothiazolyl, benzimidazolyl-, indyl, pseudoindoyl, indazolyl, quinolyl, isoquinolyl, cinnolines base, quinazolyl, quinoxalinyl, benzo dioxolyl (benzodioxolyl).As the heteroaryl of fractional saturation, what can exemplify has 1,2,3,4-tetrahydric quinoline group etc.Particularly preferably be 5-6 unit bicyclic heteroaryl, wherein be more preferably imidazolyl, thiazolyl, triazolyl, pyridyl and pyrazinyl.
Among the B, as " containing the heteroatomic 5-6 of 1～2 of being selected from O, S and N unit monocycle hetero-aromatic ring ", what can exemplify has furans, thiophene, pyrroles, imidazoles, pyrazoles, thiazole, isothiazole, azoles, pyridine, pyrimidine, pyridazine and a pyrazine ring.Preferably pyridine, pyrazine, thiphene ring; Be more preferably pyridine ring.
" can have substituent aryl ", in " can have substituent heteroaryl ", " can have the substituting group cycloalkyl ", " can have substituent cycloalkenyl group ", " can have substituent nitrogenous saturated heterocyclic ", as substituting group, have 1～5 can identical any substituting group that also can be different.Preferably be selected from the substituting group of following A group.In addition, R, R ' and R " can be identical also can be different, expression H or low alkyl group.Below identical.
The A group :-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-halogen ,-junior alkyl halides ,-low-grade alkylidene-OR ,-NO
2,-CN ,=O ,-OR ,-the O-junior alkyl halides ,-O-low-grade alkylidene-NRR ' ,-O-low-grade alkylidene-OR ,-O-low-grade alkylidene-aryl ,-SR ,-SO
2-low alkyl group ,-the SO-low alkyl group ,-COOR ,-COO-low-grade alkylidene-aryl ,-COR ,-the CO-aryl ,-aryl ,-CONRR ' ,-SO
2NRR ' ,-NRR ' ,-NR "-low-grade alkylidene-NRR ' ,-NR '-low-grade alkylidene-OR ,-NR-low-grade alkylidene-aryl ,-the NRCO-low alkyl group ,-the NRSO2-low alkyl group ,-cycloalkyl and-cycloalkenyl group.
But, R
4, R
4aAnd R
4bIn, as the substituting group of " can have substituent aryl " and " can have substituent heteroaryl ", preferably being selected from following exemplify in a)～c) substituent can identical 1～5 substituting group that also can be different.
A)-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-halogen ,-junior alkyl halides ,-low-grade alkylidene-OR ,-NO
2,-CN ,=O ,-the O-junior alkyl halides ,-SO
2-low alkyl group ,-the SO-low alkyl group ,-COOR ,-COO-low-grade alkylidene-aryl ,-COR ,-the CO-aryl ,-CONRR ' ,-SO
2NRR ' ,-Cyc or-Alp-Cyc (herein, Alp represents low-grade alkylidene, lower alkenylene or rudimentary alkynylene, Cyc represents-aryl that can be replaced by 1～5 substituting group that is selected from the A group ,-the heteroaryl that can be replaced by 1～5 substituting group that is selected from the A group ,-the nitrogenous saturated heterocyclyl that can be replaced by 1～5 substituting group that is selected from the A group ,-cycloalkyl that can be replaced by 1～5 substituting group that is selected from the A group or-cycloalkenyl group that can be replaced by 1～5 substituting group that is selected from the A group.Below identical.)。
B)-NR-E-F (herein, E represent-CO-,-COO-,-CONR '-,-SO
2NR '-or-SO
2-; F represents-Cyc or-(can be selected from low alkyl group, low-grade alkenyl or low-grade alkynyl that following group replaces :-halogen ,-NO
2,-CN ,-OR ,-O-low-grade alkylidene-NRR ' ,-O-low-grade alkylidene-OR ,-SR ,-SO
2-low alkyl group ,-the SO-low alkyl group ,-COOR ,-COR ,-the CO-aryl ,-CONRR ' ,-SO
2NRR ' ,-the NRCO-low alkyl group ,-NRR ' ,-NR '-low-grade alkylidene-OR ,-NR "-low-grade alkylidene-NRR ' with-Cyc) following identical.)
C)-Z-R ' ,-Z-Cyc ,-Z-Alp-Cyc ,-Z-Alp-Z '-R ' or-Z-Alp-Z '-Cyc (herein, Z and Z ' can be identical also can be different, expression O, S or NR.Below identical.)
Particularly preferably be ,-low-grade alkylidene-OR, CONRR ' ,-NR-CO-Cyc
1(Cyc herein,
1The aryl of expression-can be replaced by 1～5 substituting group that is selected from A group ,-heteroaryl that can be replaced by 1～5 substituting group that is selected from the A group or-the nitrogenous saturated heterocyclyl that can be replaced by 1～5 substituting group that is selected from the A group, below identical) ,-NR-SO
2-Cyc
1,-OR ,-NRR ' ,-O-low-grade alkylidene-NRR ' and-O-low-grade alkylidene-(the nitrogenous saturated heterocyclyl that can be replaced by 1～5 substituting group that is selected from A group).
When n is 2～4, a plurality of R
1Can be identical also can be different.
General formula of the present invention (I), (Ia) and (Ib) in the represented compound have as preferred compound:
(1) R
2And R
3Form-NR
2R
3Be selected from for having-OH ,=O and-compound of 1～2 substituent nitrogenous saturated heterocyclyl of low alkyl group,
(2) R
2And R
3Form-NR
2R
3Be the compound of morpholino,
(3) W is the compound of N,
(4) R
4, R
4aAnd R
4bFor-(can have substituent aryl) or-compound of (can have substituent heteroaryl),
(5) B is a phenyl ring; R
1For-low alkyl group ,-low-grade alkenyl ,-low-grade alkynyl ,-cycloalkyl ,-can have substituent aryl ,-can have substituent heteroaryl ,-halogen ,-NO
2,-CN ,-junior alkyl halides ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb or-compound of NRaCO-COORb,
(6) B is that pyridine, pyrazine or thiphene ring and n are 0 compound,
(7) X is that N, Y are that O and n are 0 compound,
(8) R
4, R
4aAnd R
4bFor having the compound that is selected from following substituent aryl :-low-grade alkylidene-OR ,-CONRR ' ,-NR-CO-Cyc
1,-NR-SO
2-Cyc
1,-OR ,-NRR ' ,-O-low-grade alkylidene-NRR ' and-O-low-grade alkylidene-(the nitrogenous saturated heterocyclyl that can be replaced by 1～5 substituting group that is selected from A group) and
(9) has the following activity (IC that suppresses of 5 μ M (micromole) in the melanoma cells proliferation inhibition test shown in the aftermentioned experimental example 3
50) compound.
As the represented particularly preferred compound of general formula (Ia), be R
4aFor have the compound that is selected from least one following substituent phenyl :-OH ,-NH
2,-NH-low alkyl group ,-N (low alkyl group)
2,-O-low-grade alkylidene-NH
2With-O-low-grade alkylidene-(the nitrogenous saturated heterocyclyl that can be replaced by low alkyl group).
In addition, have as the represented particularly preferred compound of general formula (Ib):
(1) W is N, R
4bFor-(can have substituent aryl) and R
2And R
3Form-NR
2R
3Be the compound of morpholino,
(2) B is that phenyl ring, n are 1 or 2, R
1For-halogen ,-NO
2,-CN ,-junior alkyl halides ,-ORb ,-SRb ,-NRaRb ,-NRa-CORb or-NRa-SO
2The compound of Rb, and
(3) B is that pyridine, pyrazine or thiphene ring, n are 0 and R
4bFor can be selected from-OH ,-CH
2OH and-CONH
2The compound of the phenyl that replaces of at least one substituting group,
In the The compounds of this invention,,, (Co17) 6-amino-3 '-(4-morpholino pyrido [3 ', 2 ': 4,5] furo [3,2-d] (2-pyrimidyl) nicotinanilide is arranged as the represented compound of general formula (Ia) as suitable compound; (Co33) 4-(4-morpholino pyrido [3 ', 2 ': 4,5] furo [3,2-d] (2-pyrimidyl) aniline; (Co50) 3-(4-morpholino pyrido [3 ', 2 ': 4,5] furo [3,2-d] (2-pyrimidyl)) phenol; (Co69) 4-morpholino-2-[3-(2-(1-piperazinyl) oxyethyl group) phenyl] pyrido [3 ', 2 ': 4,5] furo [3,2-d] pyrimidine; (Co73) 3 '-(4-morpholino pyrido [3 ', 2 ': 4,5] furo [3,2-d] (2-pyrimidyl) acryloyl aniline; And their salt.In addition, as the represented compound of general formula (Ib), (co-144) N-[2-(3-benzene sulfonamido phenyl)-4-morpholino (6-quinazolyl) is arranged] ethanamide; (co-164) 3-(4-morpholino pyrido [4,3-d] (2-pyrimidyl)) phenol; (Co 172) 3-(4-morpholino pyrido [3,2-d] (2-pyrimidyl) phenol; (Co-174) 3-(4-morpholino pyrido [3,4-d] (2-pyrimidyl) phenol; (Co186) 3-(6-methoxyl group-4-morpholino (2-quinazolyl)) phenol; (Co190) 3-(4-morpholino thieno-[3,2-d] (2-pyrimidine)) phenol; (Co-191) 3-(4-morpholino (2-pteridyl) phenol; And their salt.
The compounds of this invention exists geometrical isomer and tautomer sometimes, and the present invention includes separated these isomer or their mixture according to substituent kind.Therefore and there is chiral carbon atom sometimes in The compounds of this invention, has a isomer based on chiral carbon atom.The present invention includes mixture and their separated materials of these optical isomers.
In addition, The compounds of this invention forms salt sometimes.As long as the salt that allows on the pharmacopedics then has no particular limits, as acid salt, what can exemplify specifically has inorganic acid salts such as hydrochloric acid, Hydrogen bromide, hydroiodic acid HI, sulfuric acid, nitric acid, phosphoric acid; Organic acid salts such as formic acid, acetate, propionic acid, oxalic acid, propanedioic acid, succsinic acid, fumaric acid, toxilic acid, lactic acid, oxysuccinic acid, tartrate, citric acid, methylsulfonic acid, ethyl sulfonic acid, aspartic acid, L-glutamic acid.As alkali salt, the inorganic salt that metals such as containing sodium, potassium, magnesium, calcium, aluminium is arranged that can exemplify; Or organic alkali salt such as methylamine, ethamine, thanomin, Methionin, ornithine and ammonium salt etc.In addition, the present invention includes compound (I), (Ia) or (Ib) and the various hydrates of salt, solvate and polymorph material.
(manufacture method)
The following describes the typical manufacture method of The compounds of this invention.According to the kind of functional group, there be not raw material or intermediate stage to replace this functional group sometimes with suitable protecting group (promptly changing into the group of this functional group easily), this is effective on manufacturing technology.Then, remove protecting group as required, just can obtain required compound.As such functional group, can exemplify for example amino, hydroxyl, carboxyl etc.; As their protecting group, can exemplify the protecting group of record among " the Protective Groups in OrganicSynthesis (protecting group in the organic synthesis) " the 2nd edition of Greene and Wuts work for example, can suitably use these protecting groups according to reaction conditions.
The 1st manufacture method
(in the formula, L represents leavings group.Below identical.)
This manufacture method is to make the reaction of itself and amine (IV) obtain the method for The compounds of this invention (I) afterwards with ordinary method the represented compound of general formula (II) being converted into reactive derivatives (III).A ring or substituent R in reactive derivatives (III)
4On also exist under the situation of reactive site with leavings group L, as required, can be again and identical or different amine (IV) reaction.Equally, A ring or R in invention compound (I)
4On exist under the situation of chloro, leavings group L such as fluorine-based, according to J.Am.Chem.Soc., 68, the method of record in 1288 (1946), the reaction that is hydrolyzed is perhaps according to tetrahedron Lett., 40, the methods of record are reagent with the alkoxide through one's own department or unit replacement(metathesis)reaction etc. in 675 (1999), just can carry out functional group and change.
As the represented leavings group of L, organic sulfonic acid residue such as halogen or mesyloxy, tolysulfonyl oxygen base etc. preferably.
The reaction that obtains active intermediate (III) can be carried out according to ordinary method.Leavings group is the chlorine atomic time, makes in compound (II) and Phosphorus Oxychloride, oxalyl chloride or the solvent of thionyl chloride in reactionlessness or when solvent-free in cooling or under heating and reacts.As the solvent of reactionlessness, can exemplify aromatic hydrocarbon solvents such as benzene, toluene; Tetrahydrofuran (THF) (THF), 1, ether solvents such as 4-two alkane; Halogenated hydrocarbon solvent such as methylene dichloride, chloroform; Basic solvent such as pyridine, trimethylpyridine.These solvents can use separately also and can two or more mixing use.Solvent can be according to the suitably selections such as kind of starting compound.During reaction, available bases (preferably dialkyl aniline, triethylamine, ammonia, lutidine, trimethylpyridine etc.) or phosphorus chloride (for example phosphorus pentachloride), quaternary ammonium salt (for example tetraethylammonium chloride), N, N-dialkyl amide compound (for example dimethyl formamide (DMF)) is as reaction promotor.When leavings group is sulfonyloxy, can be synthetic according to ordinary method by corresponding SULPHURYL CHLORIDE, for example can be according to Tetrahedron Lett.23 (22), the methods of record are carried out in 2253 (1982), TetrahedronLett.27 (34), 4047 (1986).
Reactive derivatives (III) acts on the reaction that obtains compound (I) with amine (IV), can be by in the solvent existence of reactionlessness or not amine (IV) and compound (III) reaction being carried out.As solvent, can exemplify and aforementioned identical material, they can use separately also and can two or more mixing use.Solvent can be according to the suitably selections such as kind of starting compound.In the reaction, at mineral alkali such as sodium hydride or triethylamine (TEA), pyridine, 2, the existence of organic basess such as 6-lutidine during reaction, promotes reaction down sometimes.
The 2nd manufacture method
(in the formula, Rd represents-can have substituent low alkyl group, and the implication of Rb is with aforementioned identical.Below identical.)
This manufacture method, be according to ordinary method make general formula (Ia) or (Ic) compound that replaces of represented hydroxyl carry out the O-alkylated reaction and obtain (Ib) or (Id).Reaction method has, for example under the existence of alkali such as triethylamine, salt of wormwood, yellow soda ash, cesium carbonate, sodium hydroxide, sodium hydride, potassium tert.-butoxide, for example with haloalkyl or sulphonate etc. as alkylating reagent and compound (Ia) and (Ic) reaction.Temperature of reaction can carried out under the cooling or under the heating, according to the suitably selections such as kind of starting compound.Water for example reacts in the presence of phase-transfer catalysts such as hydrogen sulfate tetra-n-butyl ammonium as solvent or use when adding the reaction conditions of water in the O-alkylated reaction, promotes reaction sometimes.
As other method of O-alkylated reaction, can exemplify light and prolong reaction (Mitsunobu reaction) etc., for example available Synthesis, the method and the modification method thereof of 1 (1981) middle record.And when hydroxyl was carried out hydroxyethylation, the method for using the carbonic ether of [1,3] dioxolane-2-ketone also was effectively, for example available J.Am.Chem.Soc., the method for 68,781 (1946) middle records.
In addition, when having reactive functional groups on Rb, the Rd among The compounds of this invention (Ib), (Id), functional group's conversion is carried out in available known reaction.For example, when having hydroxyl on Rb, the Rd, can carry out aforesaid O-alkylated reaction; When having leavings group such as halogen, can be by carrying out N-alkylation in the method for O-alkylation in the preceding method or the record of aftermentioned the 4th manufacture method with suitable alcohol or amine reaction.When having ester group, the method for available aftermentioned the 3rd manufacture method record makes functional group change into carboxylic acid, methylol, amide group.
The starting compound of this manufacture method (Ia) and (Ic), the starting compound that available hydroxyl is protected by acyl group class protecting group (for example ethanoyl, tosyl group etc.) is made according to the method for aforementioned the 1st manufacture method record.And; with Phosphorus Oxychloride as the reaction reagent of building-up reactions derivative (III), when reaction comes synthetic (I) with required amino then; according to kind, reaction conditions and the post-treating method of raw material, protecting group, the protecting group that can remove hydroxyl generates the O-phosphamide compound sometimes.At this moment, available for example Chem.Pharm.Bull., the method for 37,2564 (1989) middle records is removed the phosphinylidyne amido.In addition, common introducing protecting group deprotection can carry out with the method for record in aforesaid " Protective Groups in Organic Synthesis (protecting group in the organic synthesis) ".
The 3rd manufacture method
(in the formula, Rf represents low alkyl group, and Rg represents to have substituent low alkyl group.Below identical.)
This manufacture method is by making the represented ester cpds of the present invention of general formula (Ie) carry out the method that functional group's conversion reaction obtains other compound methylol compound (If) of the present invention, carboxylic acid derivative (Ig), amide derivatives (Ih) respectively.The whole bag of tricks all can carry out according to ordinary method, for example method of record among " the experimental chemistry lecture " of Japanization association volume (ball is kind), aforesaid " the Protective Groups in OrganicSynthesis (protecting group in the organic synthesis) ".
Preferably, the reduction reaction that is converted into methylol compound (If) can be undertaken by use reductive agents such as lithium aluminium hydride, lithium borohydride, zinc borohydride, borine, Vitride in reaction-inert solvents such as ether solvent, aromatic hydrocarbon solvent.The hydrolysis reaction that is converted into carboxylic acid derivative (Ik) can wait and carry out by be used alone or mixed use of two or more lithium hydroxide, sodium hydroxide, potassium hydroxide in methyl alcohol, ethanol, THF, water equal solvent.The amidate action that is converted into compound (Ih) can be undertaken by for example making it after etheride (acyl chlorides etc.) or the acid anhydrides at the reactive derivatives that is converted into carboxylic acid to react with amine.When reacting with amine, preferably in the solvent of reactionlessness in alkali (mineral alkali such as sodium hydroxide; Or organic bases such as TEA, diisopropylethylamine, pyridine) carries out under the existence.More preferably, amidate action also can be by carrying out with carboxylic acid reaction in the solvent of reactionlessness under the existence of condensing agent (1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDCI), 1,1 '-carbonyl diurethane-1H-imidazoles (CDI) etc.).At this moment, also can add I-hydroxybenzotriazole additives such as (HOBt).Temperature of reaction and solvent can suitably be selected according to starting compound.
The 4th manufacture method
(in the formula, R ' is aforesaid implication, and Rh represents-can have substituent low alkyl group, Ri represents-Cyc or-can have substituent Alp.C ring represent-can have substituent nitrogenous saturated heterocyclic, and Rj represents-H ,-low alkyl group ,-aryl etc.Below identical.)
This manufacture method comprises; of the present invention nitro-compound represented at general formula (Ii) is converted into aminocompound (Ij) afterwards through reduction reaction; carry out various modification reactions such as N-alkylation, amidation, sulfuryl amine, ureaization, carbamylization, imidization or aminothiazoleization, obtain other compound of the present invention (Ik), (Im), (In), (Io), (Ip), (Iq) or (Ir) respectively.In addition, according to required, can suitably carry out known substituting group conversions such as N-alkylation again to these products.
Various reactions all can be carried out according to ordinary method.The method of record in for example available aforesaid " experimental chemistry lecture ", " protecting group in the organic synthesis ".Below exemplified preferable methods.
The reduction reaction of nitro-compound can be carried out in the presence of target-charcoal catalyzer such as (Pd-C) in alcoholic solvents such as methyl alcohol under hydrogen atmosphere.
When being raw material with various aldehyde, the N-alkylated reaction can be by using sodium borohydride, sodium triacetoxy borohydride, sodium cyanoborohydride etc. to carry out as the reductive amination process of reductive agent or by using formations imines such as Dean-Stark dewatering unit to make it then and carrying out as the method for the reactions such as sodium borohydride of reductive agent.And with haloalkyls such as iodo-methyl, bromobenzyls as raw material, when being alkylating reagent with methyl-sulfate etc., can be under cooling or heating, in the solvent that DMF, acetonitrile, toluene etc. do not participate in reacting, under the existence of alkali such as salt of wormwood, sodium hydroxide, sodium hydride, react.Monoalkylation reaction can be carried out effectively by carry out alkylation with haloalkyl according to ordinary method again after making as the amine compound acidylate of raw material with trifluoroacetyl group etc.Then with the acyl group deprotection.The dioxane glycosylation reaction can react with the haloalkyl more than 2 equivalents, also can for example be undertaken by under room temperature or heating formalin being reacted in formic acid when the diformazan glycosylation reaction.
Amidate action can carry out according to the method identical with aforementioned the 3rd manufacture method.Etheride (acyl chlorides etc.) or acid anhydrides that sulfonamide reaction can be used as response derivative carry out in the solvent of reactionlessness.The urea reaction can be by carrying out with various isocyanate reactions in the solvent that aromatic hydrocarbon solvent etc. does not participate in reacting under cooling or heating.The carboxylamine reaction can be undertaken by reacting with various chloroformate derivatives in the solvent of reactionlessness under cooling or heating.Imidization can wait with succinyl oxide, maleic anhydride and implement.
The aminothiazole reaction can be by carrying out with reactions such as α-Lu Daitongs after being converted into thiourea derivative at aminocompound (Ij).As the method that is converted into thiourea derivative, can exemplify for example Synth Commun1998,28 (8), 1451.J Org Chem, 1984,49 (6), 997.Org Synth, 1963, IV, 180.J.Am.Chem.Soc, 1934,56 1408 etc.Thiourea derivative can be by carrying out with the reaction of alpha-halogen ketone in carbonyl kind solvents such as alcoholic solvent such as ethanol or methyl ethyl ketone under cooling or the heating to the conversion of thiazole.During reaction,, reaction is carried out smoothly by adding alkali (salt of wormwood, yellow soda ash etc.).
The 5th manufacture method
(in the formula, Rk and Rm represent-can have substituent low alkyl group.)
This manufacture method is after changing into aminocompound (It) by the represented nitro-compound of the present invention of general formula (Is), carries out various modification reactions, obtains other compound of the present invention.Each reaction is undertaken by the method identical with the 4th manufacture method.
Other manufacture method
Other The compounds of this invention can be with making with above-mentioned identical manufacture method, and also the various reactions of available ordinary method are made.The method of record in for example aforementioned " experimental chemistry lecture ", " protecting group in the organic synthesis " can be suitably used in various reactions.
For example; by make the compound demethylation that has methoxyl group obtain amphyl the time; method of record in available " protecting group in the organic synthesis ", promptly under room temperature or heating in dimethyl sulfoxide (DMSO) (DMSO) equal solvent with method as reactions such as the sodium cyanide of demethylation reagent, potassium cyanide.
The manufacture method of starting compound
The starting compound of The compounds of this invention (II) is available to show that down the reaction shown in the synthesis path figure carries out according to ordinary method.
(manufacture method 1)
(in the formula, Rn represents low alkyl group.Below identical.)
Starting compound (IIc) can be by for the ring-closure reaction of the intermediate of amide compound (5) or by synthesizing through the ring-closure reaction of imidoether (6) effect for the starting compound of anthranilic acid derivative (1).Used ring-closure reaction is the ordinary method that pyrimidine ring forms reaction, and for example, the ring-closure reaction of intermediate (5) has Chem.Pharm.Bull., the method for 39 (2) 352 (1991) middle records; There is J.Med.Chem. intermediate (1) and (6) as the reaction of raw material, the method for 9,408 (1966) middle records.And, for the intermediate (5) of amide compound can be synthesized through amidation according to ordinary method by anils (4), perhaps successively (1) is carried out the esterification of carboxylic acid, amino acidylate and ester group and be converted into amide group and synthesize according to ordinary method.For example, can adopt 33,1722 (1990), Eur.J.Med.Chem.-Chim.Ther., 9 (3), 305 (1974) etc. method with reference to J.Med.Chem..With (2) is raw material when acidylate obtains (3), according to the kind and the reaction conditions of raw material, can carry out two acidylates.At this moment, by under alkaline condition, handling, just can obtain required monoacyl thing (3).
(manufacture method 2)
Starting compound (IId) can be by synthesizing as the ring-closure reaction of the intermediate (12) of amide compound or with the ring-closure reaction that amide compound (10) acts on the intermediate (7) as ester derivative.The ring-closure reaction of intermediate (12) is with aforementioned identical, as the intermediate (7) of raw material and the reaction of (10), for example can be according to J.Med.Chem., and the methods of record are carried out in 37,2106 (1994).For the intermediate (12) of amide compound can be converted and obtains by make ester cpds (7) carry out functional group with ordinary method.The intermediate (9) that is 2 cyclic ester compounds can come synthetic by form reaction with 5 yuan of rings that make nitrile compound (7) with ester cpds (8) effect in the presence of alkali.For example, can be according to J.Org.Chem.37, methods such as 3224 (1972) or J.Heterocycl.Chem.11 (6), 975 (1974) are synthesized.
(manufacture method 3)
Starting compound (IIe) for example can be synthetic by the ring-closure reaction of starting compound (14).As suitable condition, can exemplify in high boiling solvents such as phenyl ether or without the method for solvent to compound (14) heating.Starting compound (14) can be synthetic according to ordinary method.For example carrying out condensation reaction by corresponding aniline (13) and compound (15) synthesizes.
The The compounds of this invention of making thus can also can carry out the salify processing and separate purification as its salt directly with the episome form through conventional method.Separate to purify by suitably extract, concentrate, common chemical operation such as distillation, crystallization, filtration, recrystallize, various chromatographys carry out.
Various isomer can utilize the physicochemical property difference between isomer to separate with ordinary method.For example, racemic compound can change into the spatial pure isomer by common optical resolution method (for example, be converted into diastereoisomeric salt with optical activity acid (tartrate etc.) commonly used, carry out the method for optical resolution).The mixture of diastereomer for example can be by separation such as crystallization or chromatography respectively.Optically active compound can be made by suitable optical activity raw material.
Industrial applicibility
The compounds of this invention has kinase inhibiting activity, particularly PI3K and suppresses active, therefore can be used to the abnormal cell proliferation that suppresses relevant with PI3K.So, it to because of the caused disease of PI3K abnormal cell proliferation for example the therapeutical agent of restenosis, arteriosclerosis, skeletal diseases, rheumatoid arthritis, diabetic retinopathy, psoriasis, prostatomegaly, atherosclerosis, inflammation, vasculogenesis, pancreatitis, ephrosis, cancer etc. be useful.Particularly The compounds of this invention has good cancer cell multiplication restraining effect, and is all useful in the treatment of all solid carcinomas and lymphoma, particularly leukemia, skin carcinoma, bladder cancer, breast cancer, uterus carcinoma, ovarian cancer, prostate cancer, lung cancer, large bowel cancer, carcinoma of the pancreas, kidney, cancer of the stomach, cerebral tumor well to cancer.
By following pharmacological evaluation, determined the pharmacological action of The compounds of this invention.
The inhibition experiment of experimental example 1 PI3K (p110 alpha hypotype)
Mensuration is carried out with the enzyme (ox p110 α) that baculovirus expression system (expression system) makes.The preparation of enzyme is according to I Hile etc. " Cell (cell) ", and 70,419,1992 carry out.Assessing compound is mixed with the DMSO solution of 10mM (mmole), dilutes with DMSO continuously.
Assessing compound (0.5 microlitre) and enzyme are at 25 microlitre damping fluids (40mM Tris-HCl (pH 7.4), 200mM NaCl, 2mM dithiothreitol (DTT), 5mM MgCl
2) in mix after, add contain 10 microgram PI (Sigma), 2 μ Ci (microcurie) [γ-
32P] 5mM Tris-HCl (pH 7.4) damping fluid 25 microlitres of ATP (Amersham Pharmacia), 80 μ M (micromole) on-radiation ATP (Sigma), begin reaction.After 15 minutes, add the 1M HCl of 200 microlitres, the CHCl of 400 microlitres in 37 ℃ of reactions
3/ MeOH (1: 1), stirring, centrifugation.MeOH/1M HCl (1: 1) with 150 microlitres extracts organic layer twice again, with its radioactivity of Cerenkov light measurement.
The active IC of the inhibition of compound
50, be that the radioactivity when adding DMSO with list is 100%, the radioactivity when not having enzyme is 0%, the concentration of experimental compound when calculating 50% inhibition.
The compounds of this invention has good p110 alpha hypotype and suppresses active.For example,
Compound (hereinafter to be referred as Be Co) 10,
Co 17With
Co 24Has the following IC of 1 μ M
50
And, use and above-mentioned identical method, determine that The compounds of this invention also has the inhibition activity to other hypotype (for example C2 β hypotype).
The proliferation inhibition test of experimental example 2 colon-cancer cells
Colon-cancer cell strain HCT116 cell is cultivated in containing the McCoy 5A substratum (GIBCO) of 10% foetal calf serum.HCT116 (5000 cell/caves) is gone up inoculation at 96 cave plates (well plate), cultivate an evening.Compound to the ultimate density that adds therein with the substratum dilution is 0.1-30 μ M (final DMSO concentration, 1%), cultivates after 72 hours, adds Alamar Blue reagent.After 2 hours, obtain the active IC of inhibition by the fluorescence intensity ratio of excitation wavelength 530 nanometers and emission wavelength 590 nanometers
50Of the present invention
Co 14,
Co 24,
Co 25,
Co 31,
Co 46With
Co 47Compound have good cancer cell multiplication restraining effect.
The proliferation inhibition test of experimental example 3 melanoma cells
Melanoma cells strain A375 cell is cultivated in containing the DMEM substratum (GIBCO) of 10% foetal calf serum.The A375 cell is inoculated with 10000 cells/100 microlitres on the 96 cave plates that contain 1 microlitre/cave (ultimate density 0.001-30 μ M) in advance.Cultivate after 46 hours, add Alamar Blue reagent (10 microlitres/cave).After 2 hours, use and above-mentioned identical method, determine the IC of experimental compound by the fluorescence intensity ratio of excitation wavelength 530 nanometers and emission wavelength 590 nanometers
50
The compounds of this invention has good proliferation inhibition activity.For example,
Co 17,
Co 33,
Co 50,
Co 69,
Co 164,
Co 172,
Co 174,
Co 186,
Co 190With
Co 191Has good melanoma cells inhibited proliferation.Its IC
50Value is 0.33-4.26 μ M.And be 8.39 μ M as the value of the LY294002 of known PI3K inhibitor.
Except above-mentioned JEG-3, The compounds of this invention also has good cancer cell multiplication restraining effect to cervical cancer cell strain HeLa cell, lung cancer cell line A549, H460 cell, colon-cancer cell strain COLO 205, WiDr, Lovo cell, prostate cancer cell strain PC3, LNCaP cell, ovarian cancer cell strain SKOV-3, OVCAR-3, CH1 cell, neuroglial cytoma strain U87MG cell, pancreas cancer cell strain BxPC-3 cell.
Cancer cell multiplication suppresses experiment in experimental example 4 bodies
Cell 5 * 10 with human cervical carcinoma cell strain HeLaS3 strain
6The individual drosal part of being transplanted to female Balb/c nude mouse is subcutaneous.When gross tumor volume reaches 100～200 millimeters
3The time, with assessing compound 12 week of intraperitoneal administration of every day.Also in control group, 20% hydroxypropyl-beta-cyclodextrin/salt solution is carried out intraperitoneal administration.Use the vernier caliper measurement diameter of tumor, carry out till second day of final administration through the time measure.Calculate gross tumor volume by following calculating formula.
Gross tumor volume (millimeter
3)=1/2 * minor axis (millimeter)
2* major diameter (millimeter)
In this experiment, The compounds of this invention shows the cancer inhibited proliferation better than control group.
Medicine of the present invention, available a kind or two or more general formula (I), (Ia) or (Ib) shown in The compounds of this invention, to make the used medicament of preparation usually formulated according to method commonly used with carrier, vehicle and other additive.Oral forms such as administration can tablet, pill, capsule, granule, powder, liquor; Injection such as intravenous injection, intramuscular injection form; Or suppository, intranasal, carry out through mucous membrane, any form in non-oral forms such as skin.
Be used for oral solids composition as the present invention, forms such as available tablet, powder, granule.In such solids composition, one or more active substance can be mixed with at least a inert diluent, for example lactose, mannitol, glucose, hydroxypropylcellulose, Microcrystalline Cellulose, starch, polyvinylpyrrolidone, metasilicic acid magnalium.Composition also can contain the additive except that the inert thinner according to a conventional method, for example such lubricant and the so such solubility promoter of disintegrating agent, L-glutamic acid or aspartic acid of glycolic cellulose calcium of Magnesium Stearate.The sugar-coat that the also available in case of necessity sucrose of tablet or pill, gelatin, hydroxypropylcellulose, hydroxypropylmethylcellulose phthalate are such or the film of gastric solubility or enteric solubility matters are as dressing.
Be used for oral liquid composition, can comprise the emulsion that allows on the medicament, solution, suspension agent, syrup, elixir etc.; Inert diluent commonly used, for example pure water, ethanol.Said composition also can contain such auxiliary agent, sweeting agent, seasonings, perfume compound, the sanitas of wetting agent, suspension agent except that inert diluent.
As non-oral injection, comprise aseptic water-based or non-aqueous solution agent, suspension agent, emulsion.As solution, the suspension agent of water-based, contain for example distilled water for injection and physiological saline.As non-water-soluble solution, suspension agent, for example comprise propylene glycol, polyoxyethylene glycol; The vegetables oil that sweet oil is such; The alcohols that ethanol is such; Polysorbate80 etc.These compositions also can contain sanitas, wetting agent, emulsifying agent, dispersion agent, stablizer, the such auxiliary agent of solubility promoter.For example, mix sterilant or, can make it aseptic through irradiation by they are filtered through sterilization filter.Perhaps, with sterilized water or aseptic solvent for injection dissolving, they are made aseptic solids composition before use.
Common when oral, about 0.0001～50 mg/kg of the dosage of every day, preferred about 0.001～10 mg/kg, more preferably from about 0.01～1 mg/kg suits, can 1 administration, also can divide 2～4 administrations.During intravenously administrable, about 0.0001～1 mg/kg of the dosage of every day, preferred about 0.0001～0.1 mg/kg suit, but every day 1 time or divide administration several times.Dosage should be considered symptom, age, sex etc., suitably determines according to individual cases.
The compounds of this invention can use separately also and can share with other methods of treatment (for example radiotherapy and surgical operation).In addition, also can with other carcinostatic agent, for example alkylating agent (cis-platinum, carboplatin etc.), metabolic antagonist (methotrexate, 5-FU etc.), cancer resistance microbiotic (Zorubicin, bleomycin etc.), cancer resistance biology subtract (taxol, rely on pool etc.), cancer resistance hormone preparation (dexamethasone, tamoxifen etc.), cancer resistance immunity class medicament (interferon alpha, β, γ etc.) etc. and share.
The best mode that carries out an invention
Below, illustrate in greater detail the present invention with reference to embodiment.The compounds of this invention is not limited to the compound of following record.
Table 1～3 and 13～16 illustrate the starting compound that uses among the embodiment, and table 4～11 and 17～24 illustrate exemplary compounds physicochemical property of the present invention.The compounds of this invention with the chemical structural formula shown in table 12 and 25～26, the method that the method for putting down in writing in available and embodiment or the manufacture method is roughly the same or with some modification methods that those skilled in the art know is easily made.
The implication of omitting mark in the table is as follows respectively, Rco: the compound number of starting compound; Rex: the manufacture method of reference example compound (method that numeral aftermentioned reference example numbering, expression are put down in writing with this reference example or expect that identical method make this compound); Co: the compound number of The compounds of this invention; Str: structural formula; Sal: salt; Syn: (numeral aftermentioned embodiment number, expression is made this compound with the method or the method identical with it of this embodiment record to manufacture method.); DAT: physicochemical property (F:FAB-MS (M+H)
+FN:FAB-MS (M-H)
-E:EI-MS; M: fusing point [℃]; (dec.): decompose; N1:NMR (DMSO-d
6, mark in the TMS) characteristic peak δ (ppm); Ac: ethanoyl; Bn: benzyl; Ph: phenyl; The Ts:4-tosyl group; Ms: methylsulfonyl; Me: methyl; Et: ethyl.And when having a plurality of positions can be substituted base to replace, the position of substitution has been put down in writing (as, 6-MeO-7-HO: expression 6-methoxyl group-7-hydroxyl) in substituent front.
Table 1
Table 2
Table 3
Table 4
Table 5
Table 6
Table 7
Table 8
Table 9
Table 10
Table 11
Table 12
Table 13
Table 14
Table 15
Table 16
Table 17
Table 18
Table 19
Table 20
Table 21
Table 22
Table 23
Table 24
Table 25
Table 26
The manufacture method of the starting compound shown in aforementioned each table has been described below with reference to example.
Reference example 1
With the 3-methyl isophthalic acid of 2-chloro-3-cyanopyridine, ethyl glycollate and yellow soda ash-butanols suspension reflux 3 days.After distilling solvent, in the residue of gained, add entry, make it crystallization, obtain
Reference exampleization Compound (Refernce Example Compound is designated hereinafter simply as Rco) 1
Reference example 2
With the 3-methyl isophthalic acid of 2-chloro-3-cyanopyridine, glycine ethyl ester one hydrochloride and yellow soda ash-butanols suspension reflux 6 days.After distilling solvent, to the residue of gained ethyl acetate and water dilution, filter out insolubles, decompression is the organic layer of concentrated gained down.Residue is dissolved in the ethanol, adds sodium ethylate, under room temperature, stirred 15 minutes.Concentrate this reaction solution, add ethyl acetate and saturated sodium bicarbonate solution, carry out the separatory operation.This organic layer is under reduced pressure distilled solvent, and residue is purified, obtain with silica gel column chromatography
Rco 3
Reference example 3
Also in the pyridine solution of [2,3-b] pyridine-2-carboxylic acids ethyl ester, add dimethyl aminopyridine and Benzoyl chloride at the 3-aminothiophene, at room temperature stirred 18 hours, concentration of reaction solution adds 1M (mole) aqueous hydrochloric acid, uses chloroform extraction.Under reduced pressure concentrate organic layer, the residue of gained is purified, obtain with silica gel column chromatography
Rco 4
Reference example 4
Under-15 ℃
Rco 49With add Phosphorus Oxychloride in the pyridine solution of 4-nitrobenzoic acid, stirred 15 minutes in-15 ℃.On the rocks in this reaction solution, add water again, the crystallization that leaching is separated out obtains
Rco 11
Reference example 5
Rco 4Methanol solution in add the 1M aqueous sodium hydroxide solution, under room temperature, stirred 2 hours.Add the 1M aqueous hydrochloric acid, the crystallization that leaching is separated out obtains
Rco 13
Reference example 6
Rco 13Middle thionyl chloride, the reflux 2 hours of adding.After the cooling, concentration of reaction solution adds DMF and ammoniacal liquor in the residue of gained, stirred 2 hours under room temperature.Add water, use chloroform extraction.Under reduced pressure concentrate organic layer, obtain
Rco 21
Reference example 7
Rco 1The middle methane amide that adds stirred 2 hours in 200 ℃.After the cooling, the crystallization that leaching is separated out obtains
Rco 29
Reference example 8
Rco 21Methanol solution in add the 2M potassium hydroxide aqueous solution, stirred 1 hour in 100 ℃.After the cooling, add hydrochloric acid, the crystallization that leaching is separated out obtains
Roc 30
Reference example 9
Rco 36Middle acetate and 48% hydrobromic acid aqueous solution, the reflux 17 hours of adding.Under reduced pressure concentration of reaction solution adds diethyl ether, again concentrating under reduced pressure then.In the residue of gained, add sodium acetate and diacetyl oxide, stirred 2 hours in 110 ℃.The ice bath cooling down, and is on the rocks in this reaction solution, adds water again, and the crystallization that leaching is separated out obtains
Rco 38
Reference example 10
In the chloroformic solution of 3-cyano-benzoic acid methyl ester, add ethanol, be blown into hydrogen chloride gas 15 minutes in 0 ℃.Sealing was then stirred 17 hours in 0 ℃.Concentration of reaction solution adds ether, and the crystallization that leaching is separated out obtains
Rco 50
Reference example 11
In the mixture of 5-acetamido anthranilic acid, 3-nitrobenzoyl imidic acid carbethoxy hydrochloride and sodium methylate, add the 2-propyl alcohol, refluxed 3 days.Make the reaction mixture cool to room temperature, the leaching solid obtains
Rco 52
Reference example 12
Under the room temperature, in the pyridine solution of 2-amino-5-methoxy benzamide, dimethyl aminopyridine, drip the benzole soln of hexanaphthene formyl chloride, stirred 2 hours.Concentration of reaction solution is dissolved in residue in the ethyl acetate.Wash organic layer successively with 1M hydrochloric acid, saturated sodium bicarbonate aqueous solution, concentrate organic layer then, the residue of gained is dissolved in the methyl alcohol, add the 2M aqueous sodium hydroxide solution.Make the reaction mixture reflux after 2 hours, with the neutralization of 12M hydrochloric acid, distilling solvent, the leaching crystallization obtains
Rco 67
Reference example 13
In the mixture of 2-amino-5-methoxy benzamide, EDCI hydrochloride, HOBt, pyrazine carboxylic acid, add THF (tetrahydrofuran (THF)) and DMF (dimethyl formamide), under room temperature, stirred 3 days.Distill solvent, the leaching crystallization.It is dissolved in methyl alcohol and the 2M aqueous sodium hydroxide solution reflux 3 hours.With 12M hydrochloric acid neutralization reaction mixture, the crystallization that leaching generates obtains
Roc 72
Reference example 14
Rco 55Chloroform suspension in, add dimethyl aminopyridine, TEA (triethylamine), ethanol, toluene sulfonyl chloride, stirring at room 12 hours.Add DMSO and form uniform solution, stirred then 12 hours, add dimethyl aminopyridine, TEA, toluene sulfonyl chloride again, stirred 18 hours.Concentration of reaction solution dilutes residue with ethyl acetate, purifies with common method, obtains
Rco 74
Reference example 15
Rco 70Acetic acid solution in, add 48% hydrobromic acid aqueous solution, reflux 2 days.After the cooling, concentration of reaction solution adds sodium acetate and diacetyl oxide, reflux 3 hours in the residue of gained.After the cooling, concentration of reaction solution adds ether, and the leaching crystallization obtains
Rco 77
Reference example 16
Rco 60Middle sodium acetate and diacetyl oxide, the reflux 40 minutes of adding.After the cooling, the crystallization that leaching is separated out obtains
Rco 83
Reference example 17
In the methanol solution of 3-hydroxybenzene azomethine acid ethyl ester hydrochloride salt and 5-hydroxyl anthranilic acid, add sodium methylate, reflux 30 minutes.After the cooling, the crude product that leaching is separated out adds sodium acetate and diacetyl oxide, reflux 30 minutes to it.After the cooling, the crystallization that leaching is separated out obtains
Rco 92
Reference example 18
Will
Rco 52Add in the concentrated hydrochloric acid, stir down in 80 ℃.Cooled and filtered is under reduced pressure distilled filtrate, obtains 6-amino-2-(3-nitrophenyl)-3H-quinazoline-4-one hydrochloride.With in the compound of gained and after, add pyridine and dimethyl aminopyridine, add methylsulfonyl chloride again, under room temperature, stirred 20 hours.Distill solvent, the leaching crystallization obtains
Roc 95
Reference example 19
In the ethanolic soln of 2-chloro-3-cyanopyridine and ethyl glycollate, add 1,8-diazabicylo [5.4.0]-7-hendecene (DBU), reflux 21 hours.Under reduced pressure distill solvent, with the ethyl acetate dilution, water and saturated brine washing then.Under reduced pressure concentrate organic layer, make it crystallization, obtain
Rco 49
Reference example 20
Rco 96Methanol solution in, add ammoniacal liquor, under room temperature, stirred 3 hours.Under reduced pressure distill the methyl alcohol in the reaction solution, the leaching crystallization obtains
Rco 116
Reference example 21
Rco 98Methanol solution in, add ammoniacal liquor, under room temperature, stir an evening.Under reduced pressure distill the methyl alcohol in the reaction solution, the leaching crystallization obtains
Rco 117
Reference example 22
In the DMF of 3-acetoxy-benzoic acid solution, add EDCI hydrochloride and HOBt, under room temperature, stirred 10 minutes.Add 2-amino-5-methoxy benzamide then, under room temperature, stirred 1 hour.Under reduced pressure distill solvent, add entry and THF, use ethyl acetate extraction, wash with saturated brine then.Under reduced pressure distill solvent, recrystallize obtains
Rco 119
Reference example 23
Rco 105In sodium acetate, add diacetyl oxide, stirred 1 hour 15 minutes in 110 ℃.Under the cooling, the crystallization that leaching is separated out obtains
Rco 121
Reference example 24
Rco 99Two alkane solution in, add ammoniacal liquor, under room temperature, stirred 13 days.Under reduced pressure distill solvent, the leaching crystallization, obtain 3-(3-methoxy benzamide base) thiophene-2-carboxylic acid amides and
Rco 122Mixture.In the 2-of this mixture propanol solution, add the 2M aqueous sodium hydroxide solution, reflux 21 hours.The cooling post neutralization, the crystallization that leaching is separated out obtains
Rco 122
Embodiment 1
Rco 33In, add Phosphorus Oxychloride, reflux 20 minutes.Concentration of reaction solution under reduced pressure is with methylbenzene azeotropic.In the residue of gained, add morpholine, reflux 10 minutes.Under reduced pressure concentration of reaction solution with the crystallization of chloroform and water washing gained, obtains
Compound (Compoud is designated hereinafter simply as Co) 1
Embodiment 2
Co 31In the DMF solution of episome (Free form), add piperidines-1,2-dicarboxylic acid 1-benzyl ester, HOBt and EDCI hydrochloride stirred 7 hours under room temperature.Under reduced pressure distill solvent, with the ethyl acetate dilution, then with saturated sodium bicarbonate aqueous solution and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography the residue of gained is purified, make it crystallization, obtain
Co 3
Embodiment 3
Under the ice bath cooling,
Co 31In pyridine (480 milliliters) solution of episome (13.6 gram), add benzene sulfonyl chloride (6.02 milliliters), under room temperature, stirred 1.5 hours.Under reduced pressure distill solvent, the residue of gained is dissolved in the ethyl acetate, again with saturated sodium bicarbonate aqueous solution and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (elutriant; Chloroform: methyl alcohol=96: 4) residue of gained is purified, make it recrystallize (ethanol), obtain
Co 8(15.6 gram).
Embodiment 4
Under the ice bath cooling,
Co 31In THF (1 liter) solution of episome (15.3 gram), add pyridine formyl chloride (picolinoyl chloride) hydrochloride (9.40 gram) and TEA (14.7 milliliters), under room temperature, stirred 1.5 hours.Then, add pyridine formyl chloride one hydrochloride (4.00 gram) again, under room temperature, stirred 30 minutes.Under reduced pressure concentration of reaction solution is used acetic acid ethyl dissolution, then with saturated sodium bicarbonate aqueous solution and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (elutriant; Chloroform: methyl alcohol=96: 4) residue of gained is purified, make it recrystallize (ethanol), obtain
Co 10(15.4 gram).
Embodiment 5
Co 31In DMF (20 milliliters) solution of episome (300 milligrams), add 3-hydroxy-picolinic acid (140 milligrams), EDCI hydrochloride (190 milligrams) and HOBt135 milligram), under room temperature, stirred 2 hours.Under reduced pressure distill solvent, the residue of gained is dissolved among ethyl acetate and the THF, water, saturated sodium bicarbonate aqueous solution washing.Behind the anhydrous magnesium sulfate drying organic layer, under reduced pressure distill solvent, with silica gel column chromatography (elutriant; Chloroform: methyl alcohol=100: 1) residue of gained is purified, in residue obtained chloroform, methanol solution, add 4M hydrogenchloride/ethyl acetate.Under reduced pressure distill solvent, make it crystallization, obtain with methyl alcohol
Co 12(207 milligrams).
Embodiment 6
Stir down in 100 ℃
Co 31The suspension of episome (300 milligrams) and succinyl oxide (519 milligrams) and acetate (1 milliliter) 30 minutes.Under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, make it recrystallize (using methyl alcohol), obtain
Co 24(106 milligrams).
Embodiment 7
Co 18In THF of (300 milligrams) (12 milliliters) and ethanol (12 milliliters) solution, add 10%Pd-C (35 milligrams), under non-pressurized hydrogen atmosphere, in stirring at room 4 hours.Use the diatomite filtration reaction solution, concentrating under reduced pressure filtrate is used silica gel column chromatography (chloroform: methyl alcohol=98: 2～80: 20) residue of gained is purified, obtain Co 25 episomes (178 milligrams) then.In THF of this episome (153 milligrams) (35 milliliters) and methyl alcohol (20 milliliters) solution, add 1M hydrochloric acid (1.00 milliliters), under room temperature, stir, under reduced pressure distill solvent then, make it recrystallize (using methyl alcohol), acquisition dihydrochloride form
Co 25(119 milligrams).
Embodiment 8
Will in 100 ℃
Co 31The suspension of the acetate (1 milliliter) of episome (300 milligrams) and succinyl oxide (519 milligrams) stirred 30 minutes.Under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, make it recrystallize (using methyl alcohol), obtain
Co 29(57 milligrams).
Embodiment 9
Co 31In THF (60 milliliters) solution of episome (346 milligrams), add N-ethoxycarbonyl phthalic imidine (262 milligrams) and TEA (0.166 milliliter), stirred 1 day in 80 ℃.After the cooling, in reaction solution, add water, filter then, obtain
Co 30Episome (374 milligrams).In the THF of this episome (371 milligrams) (200 milliliters) solution, add 1M hydrochloric acid (1.55 milliliters), under room temperature, to stir, the crystallization that leaching is separated out obtains a hydrochloride form
Co 30(287 milligrams).
Embodiment 10
Will
Co 1(22.4 gram) and ammonium chloride (1.59 gram) are suspended in the mixed solution of ethanol (717 milliliters) and water (269 milliliters), add reduced iron (33.2 gram) then, reflux 9 hours.Take advantage of reaction solution when hot, add the THF of heat, make the crude product dissolving, use diatomite filtration.Under reduced pressure distill the major part of filtrate, the leaching crystallization of separating out then with the diethyl ether washing, obtains
Co 31Episome (18.9 gram).In THF (25 milliliters) solution of this episome (101 milligrams), add 1M hydrochloric acid (0.870 milliliter), under room temperature, stir.Methanol wash is used in the crystallization that leaching is separated out, acquisition dihydrochloride form
Co 31(75 milligrams).
Embodiment 11
Will
Rco 1Formamide soln (12 milliliters) reflux of (1.03 gram) 2 hours.The solid that cooling back leaching generates obtains
Rco 29Crude product (648 milligrams).
Rco 29In pyridine (3.5 milliliters) solution of crude product (630 milligrams), add Phosphorus Oxychloride (7 milliliters), reflux 2.5 hours.After the cooling, distill solvent.Add toluene (7 milliliters) in the residue of gained, the ice bath cooling slowly drips morpholine (7 milliliters) down, and reflux is 3.5 hours then.Add THF (3 milliliters) and morpholine (20 milliliters) again, reflux 5 days.Under reduced pressure concentration of reaction solution dilutes with ethyl acetate, and leaching coarse crystallization then with ethyl acetate, saturated sodium bicarbonate aqueous solution and water washing, makes it recrystallize (ethanol), obtains
Co 34(372 milligrams).
Embodiment 12
Rco 32Add Phosphorus Oxychloride (5 milliliters), reflux 50 minutes in (396 milligrams).Under reduced pressure distill solvent.The ice bath cooling slowly drips morpholine (10 milliliters), reflux 30 minutes to the residue of gained down.Under reduced pressure concentration of reaction solution is used the crystallization of ethyl acetate and water washing gained, makes it recrystallize (using ethanol), obtains
Co 35(411 milligrams).
Embodiment 13
Co 11In (303 milligrams), add quadrol (1.85 milliliters), stirred 2 hours in 90 ℃.Under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=80: 20) residue of gained is purified, make it crystallization (using methyl alcohol), obtain
Co 40Episome (269 milligrams).This episome (266 milligrams) is carried out the salt-forming reaction identical with embodiment 7, make the residue recrystallize (using methyl alcohol) of gained, obtain the dihydrochloride form
Co 40(153 milligrams).
Embodiment 14
Co 11In (285 milligrams), add DMF (10 milliliters),, stirred 27 hours in 80 ℃ in 110 ℃ of stirrings 2 hours.Under reduced pressure distill solvent, the residue of gained is dissolved among ethyl acetate and the THF, with sodium bicarbonate aqueous solution and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, obtain
Co 44Episome (167 milligrams).In THF of this episome (70 milligrams) (5 milliliters) and methyl alcohol (10 milliliters) solution, add 1M hydrochloric acid (0.283 milliliter), under room temperature, stir the crystallization that leaching is separated out, acquisition dihydrochloride form
Co 44(72 milligrams).
Embodiment 15
Under the ice bath cooling,
Co 31In pyridine (20 milliliters) solution of episome (297 milligrams), add Benzoyl chloride (0.118 milliliter), under room temperature, stirred 20 minutes.Under reduced pressure distill solvent, the residue of gained is dissolved in ethyl acetate and THF, with sodium bicarbonate aqueous solution and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, make the residue recrystallize (using methyl alcohol) of gained, obtain
Co 45Episome (301 milligrams).Make this episome (287 milligrams) carry out the salt-forming reaction identical, obtain a crystal of hydrochloride form with embodiment 7
Co 45(249 milligrams).
Embodiment 16
Co 48In the methyl alcohol (60 milliliters) of episome (171 milligrams) and THF (30 milliliters) solution, divide 2 times and add 1M aqueous sodium hydroxide solution (11 milliliters), under room temperature, stirred 2.5 hours.Make this reaction solution be acid with 1M hydrochloric acid, under reduced pressure distill organic solvent, the crystallization that leaching is separated out, water and ether washing.Make the coarse crystallization recrystallize (with methyl alcohol/diethyl ether) of gained, obtain
Co 49(116 milligrams).
Embodiment 17
Rco 38In (452 milligrams), add Phosphorus Oxychloride (5 milliliters), reflux 30 minutes.After the cooling, concentration of reaction solution under reduced pressure.The ice bath cooling adds THF (5 milliliters) down in the residue of gained, slowly drip morpholine (4 milliliters), removes ice bath then, reflux 1 hour.After the cooling, under reduced pressure distill solvent, the coarse crystallization of water and diethyl ether washing gained.With silica gel column chromatography (chloroform: methyl alcohol=98: 2) coarse crystallization of gained is purified, obtain
Co 50Episome (411 milligrams).Make this episome (183 milligrams) carry out the salt-forming reaction identical, make it recrystallize (using methyl alcohol), obtain a hydrochloride form with embodiment 7
Co 50(129 milligrams).
Embodiment 18
Co 50In DMF (35 milliliters) solution of episome (956 milligrams), add 4-(2-chloroethyl) morpholine hydrochloride (1.53 gram) and salt of wormwood (1.90 gram), stirred 2.5 days in 70 ℃.After the cooling, under reduced pressure distill solvent, the coarse crystallization of water and diethyl ether washing gained.With silica gel column chromatography (chloroform: methyl alcohol=98: 2) coarse crystallization of gained is purified, make it crystallization (using methyl alcohol), obtain
Co 54Episome (1.16 gram).In the solution of the THF (140 milliliters) of this episome (1.05 gram) and methyl alcohol (70 milliliters), adding 4M hydrogenchloride/ethyl acetate (1.14 milliliters) stirs under room temperature.After under reduced pressure distilling this solvent, make it recrystallize (using methyl alcohol), acquisition dihydrochloride crystallized form
Co 54(1.18 gram).
Embodiment 19
In 2-phenyl-3H-quinazoline-4-one (450 milligrams), add Phosphorus Oxychloride (5 milliliters), reflux 3 hours.Concentration of reaction solution adds saturated sodium bicarbonate aqueous solution then, uses ethyl acetate extraction.Behind the anhydrous magnesium sulfate drying organic layer, under reduced pressure distill solvent.The colourless crystallization of gained is dissolved in the benzene (10 milliliters).Add morpholine (325 milligrams).To reaction solution reflux-evening.Filter out insolubles, dilute with ethyl acetate.Wash organic layer with saturated sodium bicarbonate aqueous solution, use anhydrous magnesium sulfate drying again, under reduced pressure concentrate then.With silica gel column chromatography (benzene: ethyl acetate=5: 1) residue of gained is purified, make it recrystallize (with hexane-benzene), obtain
Co 82(136 milligrams).
Embodiment 20
Co 84In the DMSO of (190 milligrams) (5 milliliters) solution, add sodium cyanide (132 milligrams), stirred 2 hours in 180 ℃.After the cooling, in reaction solution, add water, use ethyl acetate extraction, wash organic layer, use anhydrous sodium sulfate drying, filter then, under reduced pressure distill solvent with saturated brine.Make the residue recrystallize (hexane/ethyl acetate) of gained, obtain
Co 92(40 milligrams).
Embodiment 21
Co 85In the acetate of (500 milligrams) (12 milliliters) solution, add iron (415 milligrams), stirred 1 hour in 105 ℃.After the cooling, in reaction solution, add the chloroform and the 1 molar sodium hydroxide aqueous solution.Use diatomite filtration, use chloroform extraction.Organic layer washs with saturated brine, uses anhydrous sodium sulfate drying, and filters, and under reduced pressure distills solvent then.In the residue of gained, add 1M hydrochloric acid (10 milliliters), stirred 90 minutes in 85 ℃.After the cooling, add the 1M aqueous sodium hydroxide solution, use chloroform extraction, wash organic layer with saturated brine.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=50: 1) residue of gained is purified, make it recrystallize (chloroform/hexane), obtain
Co 97(374 milligrams).
Embodiment 22
Co 97In the formic acid of (149 milligrams) (3 milliliters) solution, add diacetyl oxide (3 milliliters), under room temperature, stirred 2 hours.Add water, use ethyl acetate extraction, with saturated sodium bicarbonate aqueous solution and saturated brine washing organic layer.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=50: 1) residue is purified, make it recrystallize (with chloroform/hexane), obtain
Co 98(46 milligrams).
Embodiment 23
Rco 74In (270 milligrams), add Phosphorus Oxychloride (3 milliliters), reflux 0.5 hour.The concentrating under reduced pressure reaction solution adds morpholine (10 milliliters).To reaction solution reflux 1 hour, concentrating under reduced pressure diluted with ethyl acetate then.Wash organic layer with saturated sodium bicarbonate aqueous solution, use anhydrous magnesium sulfate drying, carry out concentrating under reduced pressure then.With silica gel column chromatography (elutriant; Hexane: ethyl acetate=5: 1) purify, add ethanol (2 milliliters), 20% potassium hydroxide aqueous solution (100 milligrams), at room temperature stirred 40 minutes.Use ethyl acetate extraction, wash organic layer with saturated sodium bicarbonate aqueous solution.Behind anhydrous magnesium sulfate drying, carry out concentrating under reduced pressure.Crystallization with the mixed solvent of ethyl acetate-hexane washs gained makes it recrystallize (using ethyl acetate/hexane) then, obtains
Co 99(30 milligrams).
Embodiment 24
Co 86In the toluene of (95 milligrams) (15 milliliters) solution, add sodium hydroxide (43 milligrams), salt of wormwood (37 milligrams) and hydrogen sulfate tetra-n-butyl ammonium (2 milligrams), stirred 30 minutes in 35 ℃.Add methyl-sulfate (34 milligrams) again, stirred 2 hours in 35 ℃.Filtering reacting liquid under reduced pressure distills solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=20: 1) residue is purified, make it recrystallize (with chloroform/hexane), obtain
Co 105(62 milligrams).
Embodiment 25
Co 97In the chloroform of (200 milligrams) (6 milliliters) solution, add Tosyl chloride (124 milligrams) and pyridine (1 milliliter), under room temperature, stirred 45 minutes.Add 1M hydrochloric acid, use ethyl acetate extraction, with saturated sodium bicarbonate aqueous solution and saturated brine washing organic layer.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.Make residue recrystallize (with chloroform/hexane), obtain
Co 106(165 milligrams).
Embodiment 26
Co 97In (250 milligrams), add 35% the morpholine aqueous solution (5 milliliters) and formic acid (5 milliliters), stirred 90 minutes in 100 ℃.After the cooling, add the 1M aqueous sodium hydroxide solution, use ethyl acetate extraction, wash organic layer with saturated brine.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Hexane: ethyl acetate=4: 1) residue is purified, make it recrystallize (with chloroform/hexane), obtain
Co 107(133 milligrams).
Embodiment 27
Rco 76In (6.2 gram), add Phosphorus Oxychloride (50 milliliters), reflux 1 hour.Behind the concentrating under reduced pressure reaction solution, it is dissolved in chloroform.Wash chloroform layer 2 times with saturated sodium bicarbonate aqueous solution, use anhydrous magnesium sulfate drying, concentrating under reduced pressure obtains 6.0 gram crystallizations then.In therein 802 milligrams, add thiomorpholine (500 milligrams), benzene (10 milliliters).In 70 ℃ the reaction solution heated and stirred after 1 hour, is diluted with ethyl acetate.With saturated sodium bicarbonate aqueous solution and saturated brine washing organic layer, use anhydrous magnesium sulfate drying again, carry out concentrating under reduced pressure then.Purify with silica gel column chromatography (hexane-ethyl acetate=5: 1), obtain tosic acid 4-thiomorpholine generation-2-phenyl (6-quinazolyl) ester (828 milligrams).Wherein 802 milligrams are dissolved among methyl alcohol (10 milliliters) and the THF (10 milliliters), add 20% potassium hydroxide aqueous solution (1.0 gram), stirred 1 hour in 70 ℃.Add entry and 1M hydrochloric acid neutralizes, use ethyl acetate extraction then.Wash organic layer with saturated brine.With behind the anhydrous magnesium sulfate drying, carry out concentrating under reduced pressure again.Make it recrystallize (with ethyl acetate-hexane), obtain
Co 108(151 milligrams).
Embodiment 28
In acetate 2-methyl-4-oxo-4H-benzo [d] [1,3] (6- piperazine base) ester (3 gram), add ammonium acetate (1.2 gram), stirred 30 minutes in 150 ℃.After being cooled to 80 ℃, add methyl alcohol, stirred 1 hour in 80 ℃.After the cooling, methanol wash is used in the crystallization that leaching is separated out, and obtains crystallization (930 milligrams).In the DMSO of gained crystallization (918 milligrams) (10 milliliters)/chloroform (5 milliliters) solution, add the dimethyl aminopyridine of toluene sulfonyl chloride (1 milliliter), TEA (1 milliliter) and catalytic amount, under room temperature, stirred 8 hours.Use ethyl acetate extraction, with saturated sodium bicarbonate aqueous solution and saturated brine washing organic layer.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.In the residue of gained, add Phosphorus Oxychloride (15 milliliters), reflux 15 hours.After the cooling, under reduced pressure distill Phosphorus Oxychloride.Use chloroform extraction, wash organic layer with saturated sodium bicarbonate aqueous solution.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=50: 1) residue is purified, obtain product liquid (577 milligrams).In its toluene (20 milliliters) solution, add morpholine (2 gram), reflux 16 hours.After the cooling, under reduced pressure distill solvent.In residue obtained ethanol (15 milliliters) solution, add 20% potassium hydroxide aqueous solution (1 milliliter), under room temperature, stirred 1 hour.Under reduced pressure distill solvent, with silica gel column chromatography (elutriant; Chloroform: methyl alcohol=20: 1) residue is purified, make it recrystallize (with chloroform/methanol/hexane), obtain
Co 109(207 milligrams).
Embodiment 29
Rco 78In (590 milligrams), add Phosphorus Oxychloride (10 milliliters), reflux 0.5 hour.Concentration of reaction solution with the chloroform dilution, washs with saturated sodium bicarbonate aqueous solution.Behind the anhydrous magnesium sulfate drying organic layer, under reduced pressure distill solvent.In the colourless crystallization of gained, add morpholine (10 milliliters), reflux 12 hours.Reaction solution dilutes with chloroform, after water, saturated sodium bicarbonate aqueous solution washing, uses anhydrous magnesium sulfate drying.Under reduced pressure concentrate the organic layer of gained, make the residue crystallization with chloroform-methanol.Recrystallize (with ethyl acetate-hexane) obtains
Co 110(126 milligrams).
Embodiment 30
Rco 67In (957 milligrams), add acetate (20 milliliters), 48% hydrobromic acid aqueous solution (20 milliliters), stirred 13 hours down for 135 ℃ in oil bath temperature.Behind the cool to room temperature, leaching is the crystallization of the mixture of raw material and demethylation body.In the crystallization of gained, add diacetyl oxide (30 milliliters), sodium acetate (112 milligrams), reflux 30 minutes.After the cooling, the leaching crystallization.In the crystallization of gained, add Phosphorus Oxychloride (10 milliliters), reflux 30 minutes.Carry out concentrating under reduced pressure, the residue of gained is dissolved in the chloroform, wash with saturated sodium bicarbonate aqueous solution.Behind anhydrous magnesium sulfate drying, carry out concentrating under reduced pressure.In the residue of gained, add morpholine (20 milliliters), reflux 15 hours.The concentrating under reduced pressure reaction solution.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=50: 1) purify, the crystallization with the mixed solvent of chloroform-ether washs gained obtains
Co 127(193 milligrams).
Embodiment 31
Co 111In the acetate of (500 milligrams) (12 milliliters) solution, add iron (396 milligrams), stirred 45 minutes in 105 ℃.After the cooling, in reaction solution, add chloroform and 1M aqueous sodium hydroxide solution.Use diatomite filtration, use chloroform extraction again.Wash organic layer with saturated brine, with behind the anhydrous sodium sulfate drying, filter again, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=10: 1) to residue obtained purification, make it recrystallize (chloroform/methanol/hexane), obtain
Co 129(120 milligrams).
Embodiment 32
Co 116In the ethanol of (564 milligrams) (8 milliliters)/THF (8 milliliters) solution, add 1M aqueous sodium hydroxide solution (8 milliliters), under room temperature, stirred 15 hours.Add 1M hydrochloric acid (8 milliliters), use extracted with diethyl ether.Wash organic layer with saturated brine, with behind the anhydrous sodium sulfate drying, filter again, under reduced pressure distill solvent.(methanol/hexane obtains to make the residue recrystallize
Co 130(163 milligrams).
Embodiment 33
Co 117In the THF of (325 milligrams) (40 milliliters) solution, add lithium aluminium hydride (67 milligrams), stirred 2 hours in 0 ℃.Add entry (0.1 milliliter), 1M aqueous sodium hydroxide solution (0.1 milliliter) and water (0.3 milliliter) successively.Under room temperature, stirred 30 minutes.Behind anhydrous sodium sulfate drying,, under reduced pressure distill solvent by filtered through silica gel.Make residue recrystallize (using the THF/ hexane), obtain
Co 131(158 milligrams).
Embodiment 34
Will
Co 112(860 milligrams) are dissolved in the mixed solvent of THF (30 milliliters), methyl alcohol (30 milliliters) and ethanol (30 milliliters), add 10% Pd-C (130 milligrams), under the normal pressure hydrogen atmosphere, stir 2 hours under room temperature.Filter out insolubles, distill solvent, obtain 780 milligrams solid.Make 202 milligrams of recrystallize (with ethanol/methyl alcohol) wherein, obtain
Co 133(148 milligrams).
Embodiment 35
Will
Co 133(202 milligrams) are dissolved in the pyridine (10 milliliters), add methylsulfonyl chloride (96 milligrams) under room temperature.Stir after 15 hours, under reduced pressure distill solvent.The residue of gained is dissolved in the ethyl acetate, washes organic layer with water.Behind anhydrous magnesium sulfate drying, under reduced pressure distill solvent.With silica gel column chromatography (chloroform-methanol=100: 1) coarse crystallization of gained is purified, make it recrystallize (with ethanol-ethyl acetate-hexane), obtain
Co 135
Embodiment 36
Co 131In the DMF of (177 milligrams) (12 milliliters) solution, add HOBt (75 milligrams) and EDCI hydrochloride (106 milligrams),, under room temperature, stirred 30 minutes in 0 ℃ of stirring 30 minutes.Add ammoniacal liquor (2 milliliters), under room temperature, stirred 3 hours.Use chloroform extraction, wash organic layer with water.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform/methanol=10: 1) residue is purified, make it recrystallize (chloroform/methanol/hexane), obtain
Co 136(39 milligrams).
Embodiment 37
Rco 87In (11 gram), add Phosphorus Oxychloride (15 milliliters), reflux 1 hour.After the cooling, under reduced pressure distill Phosphorus Oxychloride.Use chloroform extraction, wash organic layer with saturated sodium bicarbonate aqueous solution.Behind anhydrous sodium sulfate drying, filter, under reduced pressure distill solvent.Add morpholine (5 gram) in residue obtained toluene (40 milliliters) solution, reflux 17 hours after the cooling, under reduced pressure distills solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=30: 1) residue is purified, make it recrystallize (chloroform/ether/hexane), obtain
Co 138(869 milligrams).
Embodiment 38
Co 129In the DMF of (457 milligrams) (10 milliliters) solution, add diacetyl oxide (0.75 milliliter) and pyridine (1 milliliter), under room temperature, stirred 1 hour.Add 1M aqueous sodium hydroxide solution (15 milliliters) and water, use chloroform extraction.Behind the anhydrous sodium sulfate drying organic layer, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=10: 1) residue is purified, make it recrystallize (with chloroform/methanol/hexane), with the ether washing, obtain again
Co 139(358 milligrams).
Embodiment 39
Co 133In (476 milligrams), add benzene (10 milliliters), phenyl aldehyde (249 milligrams) and THF (10 milliliters) successively, slowly distill solvent, reflux is 2 hours simultaneously.Under reduced pressure distill solvent, the residue of gained is dissolved in the methyl alcohol (20 milliliters).The ice bath cooling adds sodium borohydride (50 milligrams) down, stirs 1 hour under room temperature.Under reduced pressure distill solvent, residue is dissolved in the ethyl acetate.Organic layer is water, saturated brine washing successively, then with anhydrous magnesium sulfate drying.Under decompression, distill solvent again, with silica gel column chromatography (chloroform: methyl alcohol=100: 1) residue is purified, make it recrystallize (ethyl acetate/hexane), obtain
Co 140(259 milligrams).
Embodiment 40
Will
Co 133(3.0 gram) is dissolved in the pyridine (50 milliliters), adds benzene sulfonyl chloride (1.9 gram) under room temperature.Stir after 2 hours, under reduced pressure distill solvent.In the residue of gained, add ethyl acetate and water, wash organic layer 3 times with saturated brine.Behind the organic layer with the anhydrous magnesium sulfate drying gained, under reduced pressure distill solvent.With silica gel column chromatography (chloroform: methyl alcohol=100: 1) coarse crystallization of gained is purified, make it recrystallize (using ethanol), obtain
Co 141(3.0 gram).
Embodiment 41
Co 133In (540 milligrams), add THF (15 milliliters), phenylcarbimide (207 milligrams).Reflux 3 hours adds phenylcarbimide (500 milligrams), reflux 4 hours once more.Add 1M aqueous sodium hydroxide solution (5 milliliters), stir after 15 minutes, add 1M hydrochloric acid (5 milliliters) and neutralize.Use the chloroform extraction reaction solution, behind anhydrous magnesium sulfate drying, under reduced pressure distill solvent.With silica gel column chromatography (chloroform: methyl alcohol=50: 1) residue of gained is purified, make it recrystallize (with 2-propyl alcohol/diethyl ether/hexane), obtain
Co 148(180 milligrams).
Embodiment 42
Co 133In (440 milligrams), add THF (15 milliliters) and TEA (520 milligrams).Under room temperature, drip phenyl chloroformate (498 milligrams), under room temperature, stirred 2 hours.After adding methyl alcohol, the ice bath cooling adds 1 molar sodium hydroxide (5 milliliters) down, stirs 20 minutes, adds 1M hydrochloric acid (5 milliliters) and neutralizes, and uses the chloroform extraction reaction solution, again with behind the anhydrous magnesium sulfate drying, under reduced pressure distills solvent.With silica gel column chromatography (chloroform: methyl alcohol=50: 1) residue of gained is purified, make it recrystallize (ethyl acetate), obtain
Co 149(189 milligrams).
Embodiment 43
Co 133In the THF of (253 milligrams) (10 milliliters) solution, add different nicotinoyl chlorine hydrochloride (280 milligrams) and pyridine (0.127 milliliter), under room temperature, stirred 5.5 hours, add TEA (0.1 milliliter) again, under room temperature, stirred 2.5 hours.After this, add 1M aqueous sodium hydroxide solution (0.786 milliliter) and methyl alcohol (4 milliliters), under room temperature, stirred 30 minutes, make the ester hydrolysis.After the neutralization, under reduced pressure distill most of solvent, the coarse crystallization that leaching is separated out with ethyl acetate and water washing crystallization, makes the coarse crystallization recrystallize (using ethanol) of gained, obtains
Co 150(71 milligrams).
Embodiment 44
Co 97In the chloroform of (285 milligrams) (12 milliliters) solution, add chlorine oxo ethyl acetate (190 milligrams) and TEA (1 milliliter), under room temperature, stirred 16 hours.Use chloroform extraction, wash organic layer with water.Behind anhydrous magnesium sulfate drying, filter, under reduced pressure distill solvent.With silica gel column chromatography (elutriant; Chloroform: methyl alcohol=50: 1) residue is purified, make it recrystallize (with chloroform/methanol/hexane), obtain
Co 159(103 milligrams).
Embodiment 45
Under the ice bath cooling,
Co 97In chloroform (30 milliliters) solution of (1.2 gram), add isothiocyanic acid benzoyl ester (1.2 milliliters), under room temperature, stirred 3 hours.The crystallization that leaching generates.Methylamine/the methanol solution of adding 40% in the crystallization of gained stirred 1 hour under room temperature.The concentrating under reduced pressure reaction solution is purified with silica gel column chromatography, obtains 1-(4-morpholino-2-phenyl (6-quinazolyl) thiocarbamide (1.1 gram).In therein 266 milligrams, add the monochloroacetaldehyde aqueous solution (300 milligrams) of ethanol (5 milliliters), methyl alcohol (3 milliliters) and 40%, stirred 4 days.Use the ethyl acetate dilute reaction solution,, use anhydrous magnesium sulfate drying with the saturated sodium bicarbonate aqueous solution washing.With silica gel column chromatography (hexane: ethyl acetate=2: 1), make it recrystallize (using ethanol/hexane), obtain to after the residue purification
Co 160(49 milligrams).
Embodiment 46
Co 91In (500 milligrams), add acetate (5 milliliters), 48% hydrobromic acid aqueous solution (5 milliliters), reflux 13 hours.Distill solvent, with in 1M aqueous sodium hydroxide solution and the saturated sodium bicarbonate aqueous solution and after, use ethyl acetate extraction.Behind the anhydrous magnesium sulfate drying organic layer, carry out concentrating under reduced pressure.With silica gel column chromatography (hexane: ethyl acetate=1: 1) coarse crystallization of gained is purified, make it recrystallize (using ethanol), obtain
Co 162(112 milligrams).
Embodiment 47
In the THF (20 milliliters) of diethylazodicarboxylate's (0.101 milliliter) and triphenyl phosphine (168 milligrams) solution, add 3-morpholino propyl alcohol (93 milligrams) and
CO 50Episome (203 milligrams), stirred 13 hours down in 60 ℃.Add diethylazodicarboxylate's (0.1 milliliter) and triphenyl phosphine (170 milligrams) and 3-morpholino propyl alcohol (93 milligrams) again, stir down in 60 ℃.Carry out this operation once more.After the cooling, add entry and ethyl acetate, make reaction solution be alkalescence with saturated sodium bicarbonate aqueous solution.Behind ethyl acetate extraction, wash with saturated brine.Use anhydrous sodium sulfate drying again, under reduced pressure distill solvent then, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) to residue obtained purification, make it recrystallize (using methyl alcohol), obtain
Co 58Episome (174 milligrams).Make this episome (71 milligrams) carry out the salt-forming reaction identical, make it recrystallize (using methyl alcohol), obtain hydrochloride form with embodiment 18
Co 58(68 milligrams).
Embodiment 48
Co 61In the methyl alcohol (15 milliliters) of (1.48 gram) and the mixing solutions of water (15 milliliters), add salt of wormwood (1.10 gram), after 80 ℃ of stirrings, add methyl alcohol (8 milliliters) and water (8 milliliters) again, stirred 12 hours in 80 ℃.After the cooling, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) coarse crystallization of leaching gained is purified, make it crystallization (using methyl alcohol), obtain
Co 59Episome (1.13 gram).Make this episome (160 milligrams) carry out the salt-forming reaction identical, make it recrystallize (using methyl alcohol), obtain the dihydrochloride form with embodiment 18
Co 59(146 milligrams).
Embodiment 49
Under the ice bath cooling,
Co 31In pyridine (70 milliliters) solution of episome (2.21 gram), add trifluoroacetic anhydride (1.07 milliliters) and dimethyl aminopyridine (78 milligrams), stir after 1 hour, add trifluoroacetic anhydride (0.5 milliliter) and dimethyl aminopyridine (30 milligrams) again, stirred 1 hour down in the ice bath cooling.Under reduced pressure distill solvent, add entry and ethyl acetate, the crystallization that leaching is separated out with the ethyl acetate washing, obtains
Co 60(2.66 gram).
Embodiment 50
Co 50In the episome (1.29 gram), add entry (0.645 milliliter), ethylene dibromide (1.11 milliliters), hydrogen sulfate TBuA (22 milligrams) and 2M aqueous sodium hydroxide solution (2.58 milliliters), stirred 6 hours in 60 ℃.In reaction solution, add chloroform, filter out insolubles, use chloroform extraction filtrate, wash with saturated brine then.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, obtain
Co 62(376 milligrams).
Embodiment 51
Co 62In the DMF of (211 milligrams) (5 milliliters) solution, add 1-methylpiperazine (139 milligrams) and salt of wormwood (256 milligrams), stirred 4 hours in 60 ℃.Under reduced pressure distill solvent, in the residue of gained, add entry and THF, behind ethyl acetate extraction, under reduced pressure distill solvent.With silica gel column chromatography (chloroform: methyl alcohol=97: 3～95: 5) residue of gained is purified, obtain
Co 64Episome (198 milligrams).Make this episome (198 milligrams) carry out the salt-forming reaction identical, make it recrystallize (using methyl alcohol), obtain the tri hydrochloride form with embodiment 18
Co 64(160 milligrams).
Embodiment 52
Co 62In the DMF of (232 milligrams) (5 milliliters) solution, add piperazine-1-carboxylic acid tert-butyl ester (285 milligrams) and salt of wormwood (282 milligrams), stirred 17 hours in 60 ℃.Under reduced pressure distill solvent, in the residue of gained, add water, use ethyl acetate extraction, wash with saturated brine then.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=99: 1) residue of gained is purified, obtain coarse crystallization (227 milligrams).In the two alkane (3 milliliters) and methyl alcohol (3 milliliters) solution of this coarse crystallization (212 milligrams), add 4M hydrogenchloride/ethyl acetate (1 milliliter), under room temperature, stirred 4 hours.Concentration of reaction solution makes residue recrystallize (using methyl alcohol), obtains
Co 69(144 milligrams).
Embodiment 53
Co 59In THF (3 milliliters) solution of episome (216 milligrams), add Paraformaldehyde 96 (15 milligrams) and acetate (81 milliliters), under room temperature, stirred 10 minutes, add sodium triacetoxy borohydride (199 milligrams) then, under room temperature, stirred 21 hours.After this, divide 3 times and add formaldehyde liquid (0.44 milliliter), acetate (5.5 milliliters) and sodium triacetoxy borohydride (704 milligrams), under room temperature, stirred 4 days.With 2M aqueous sodium hydroxide solution neutralization reaction liquid, add THF again, behind ethyl acetate extraction, wash with saturated brine.Use anhydrous sodium sulfate drying, under reduced pressure distill solvent then, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, obtain
Co 70Episome (162 milligrams).Make this episome (48 milligrams) carry out the salt-forming reaction identical, make it recrystallize (using methyl alcohol), obtain the dihydrochloride form with embodiment 18
Co 70(53 milligrams).
Embodiment 54
Will in 100 ℃
Co 50Episome (322 milligrams), 1,3-dioxolane-2-ketone (814 milligrams) and salt of wormwood (192 milligrams) stirred 2 hours, added 1 again, and 3-dioxolane-2-ketone (680 milligrams) stirred 17 hours in 100 ℃.After this, add DMF (3 milliliters) and stirred 2 hours, add 1 again, 3-dioxolane-2-ketone (670 milligrams) stirred 20 hours in 100 ℃.After the cooling, under reduced pressure distill solvent, add water, then add the 1 mole hydrochloride aqueous solution up to not producing bubble.The coarse crystallization that leaching is separated out makes it recrystallize (using methyl alcohol), obtains
Co 77(164 milligrams).
Embodiment 55
Rco 48In (1.07 gram), add Phosphorus Oxychloride (10 milliliters), reflux 2.5 hours.Under reduced pressure distill solvent, with methylbenzene azeotropic.In the residue of gained, add THF (15 milliliters), the ice bath cooling slowly drips morpholine (10 milliliters) down, removes ice bath then, reflux 30 minutes.In reaction solution, add ethyl acetate and THF, water and saturated brine washing.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=98: 2) residue of gained is purified, obtain 2-(4-morpholino pyrido [3 ', 2 ': 4,5] furo [3,2-d] (2-pyrimidyl) phenyl-phosphonic acid two (morpholino acid amides) (594 milligrams).In this compound (360 milligrams), add formic acid (4 milliliters), stirred 3 days in 100 ℃.Under reduced pressure distill solvent, add ethyl acetate and water, under the ice bath cooling, neutralize with saturated sodium bicarbonate aqueous solution.The crystallization that leaching is separated out obtains crystallization (162 milligrams).Make crystallization (123 milligrams) recrystallize (the usefulness methyl alcohol-THF), obtain of gained
Co 79(122 milligrams).
Embodiment 56
Co 80In (220 milligrams), add two alkane (3.9 milliliters) and 6M hydrochloric acid (5.5 milliliters), reflux 3 days.The cooling post neutralization with the mixing solutions extraction of ethyl acetate and THF, washs with saturated brine.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, with silica gel column chromatography (chloroform: methyl alcohol=96: 4) residue of gained is purified, obtain crystallization (83 milligrams).Make crystallization (81 milligrams) recrystallize (using THF-methyl alcohol) of gained, obtain
Co 81(53 milligrams).
Embodiment 57
Make under the ice bath cooling
Co 168Pyridine (9 milliliters) the solution cooling of episome (151 milligrams) adds diacetyl oxide (4.5 milliliters), stirs under the ice bath cooling.After reaction finishes, reaction solution is injected frozen water, use ethyl acetate extraction, wash with saturated brine again.Behind anhydrous sodium sulfate drying, under reduced pressure distill solvent, obtain
Co 183Episome (158 milligrams).Make this episome (156 milligrams) carry out the salt-forming reaction identical, make the crystallization recrystallize (using methyl alcohol) of acquisition, obtain a hydrochloride form with embodiment 18
Co 169(93 milligrams).
Embodiment 58
In the DMF of 60% sodium hydride (63 milligrams) (5 milliliters) solution, drip 2-morpholino ethanol (806 milligrams), under room temperature, stirred 15 minutes.Then add
Co 179Episome (285 milligrams) stirred 23 hours in 60 ℃.After this, in the DMF of 60% sodium hydride (63 milligrams) (1 milliliter) solution, drip 2-morpholino ethanol (806 milligrams), stirred 15 minutes under room temperature, preparation feedback liquid drips this reaction solution to above-mentioned reaction mixture, in 60 ℃ of stirrings in addition.Carry out 3 these operations.Under reduced pressure distill solvent, in the residue of gained, add entry and THF, behind ethyl acetate extraction, wash with saturated brine.Use anhydrous sodium sulfate drying, under reduced pressure distill solvent then, with silica gel column chromatography (chloroform: methyl alcohol=95: 5) residue of gained is purified, obtain
Co 192Episome (529 milligrams).Make this episome (404 milligrams) carry out the salt-forming reaction identical, make the crystallization recrystallize (using methyl alcohol) of gained, obtain the dihydrochloride form with embodiment 18
Co 192(320 milligrams).
Claims (8)
1. by condensed heteroaryl derivatives or its salt of following general formula (Ib) expression,
Mark in the formula is represented following implication
B: phenyl ring or contain the heteroatomic 5-6 of 1～2 of being selected from O, S and N unit monocycle hetero-aromatic ring,
R
1:-C
1～6Alkyl ,-C
2～6Thiazolinyl ,-C
2～6Alkynyl ,-C
3～8Cycloalkyl ,-can have 1～5 substituent C that is selected from the A group
6～14Aryl ,-can have 1～5 substituent heteroaryl that is selected from A group ,-halogen ,-NO
2,-CN ,-halo C
1～6Alkyl ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb ,-NRaCO-COORb ,-NRaCOORb ,-NRaCO-C
1～6Alkylidene group-C
6～14Aryl ,-NRa-SO
2-C
1～6Alkylidene group-C
6～14Aryl ,-NRa-C
1～6Alkylidene group-C
6～14Aryl ,-C
1～6Alkylidene group-ORb ,-C
1～6Alkylidene group-NRaRb ,-the nitrogenous saturated heterocyclyl of CO-,-CONRa-C
1～6Alkylidene group-ORb ,-CONRa-C
1～6Alkylidene group-NRcRb ,-CONRa-C
1～6Alkylidene group-nitrogenous saturated heterocyclyl ,-O-C
1～6Alkylidene group-ORb ,-O-C
1～6Alkylidene group-NRaRb ,-O-C
1～6Alkylidene group-nitrogenous saturated heterocyclyl ,-O-C
1～6Alkylidene group-O-C
1～6Alkylidene group-ORb ,-O-C
1～6Alkylidene group-O-C
1～6Alkylidene group-NRaRb ,-O-C
1～6Alkylidene group-NRc-C
1～6Alkylidene group-NRaRb ,-NRc-C
1～6Alkylidene group-NRaRb ,-N (C
1～6Alkylidene group-NRaRb)
2,-CONRa-ORb ,-NRa-CO-NRbRc or-OCORb,
The A group comprises :-C
1～6Alkyl ,-C
2～6Thiazolinyl ,-C
2～6Alkynyl ,-halogen ,-halo C
1～6Alkyl ,-C
1～6Alkylidene group-OR ,-NO
2,-CN ,=O ,-OR ,-O-halo C
1～6Alkyl ,-O-C
1～6Alkylidene group-NRR ' ,-O-C
1～6Alkylidene group-OR ,-O-C
1～6Alkylidene group-C
6～14Aryl ,-SR ,-SO
2-C
1～6Alkyl ,-SO-C
1～6Alkyl ,-COOR ,-COO-C
1～6Alkylidene group-C
6～14Aryl ,-COR ,-CO-C
6～14Aryl ,-C
6～14Aryl ,-CONRR ' ,-SO
2NRR ' ,-NRR ' ,-NR "-C
1～6Alkylidene group-NRR '-,-NR '-C
1～6Alkylidene group-OR ,-NR-C
1～6Alkylidene group-C
6～14Aryl ,-NRCO-C
1～6Alkyl ,-NRSO
2-C
1～6Alkyl ,-C
3～8Cycloalkyl and-C
3～8Cycloalkenyl group; Wherein R, R ' and R " can be identical also can be different, expression H or C
1～6Alkyl,
R
2And R
3: with the N atom of adjacency be connected to-NR
2R
3Be selected from for having 1～2-OH ,=O and C
1～6The substituent nitrogenous saturated heterocyclyl of alkyl,
Ra and Rc: can be identical also can be different, for-H or-C
1～6Alkyl,
Rb: for-H ,-C
1～6Alkyl ,-C
3～8Cycloalkyl ,-can have 1～5 substituent C that is selected from the A group
6～14Aryl or-can have 1～5 substituent heteroaryl that is selected from A group,
N:0,1,2 or 3, but n is 1,2 or 3 when B is phenyl ring,
R
4b: for-(can have 1～5 and be selected from A
4The substituent C of group
6～14Aryl),
A
4Group comprises a) :-C
1～6Alkyl ,-C
2～6Thiazolinyl ,-C
2～6Alkynyl ,-halogen ,-halo C
1～6Alkyl ,-C
1～6Alkylidene group-OR ,-NO
2,-CN ,=O ,-O-halo C
1～6Alkyl ,-SO
2-C
1～6Alkyl ,-SO-C
1～6Alkyl ,-COOR ,-COO-C
1～6Alkylidene group-C
6～14Aryl ,-COR ,-CO-C
6～14Aryl ,-CONRR ', SO
2NRR ' ,-Cyc or-Alp-Cyc, herein, Alp represents C
1～6Alkylidene group, C
2～6Alkenylene or C
2～6Alkynylene, Cyc are represented can be by 1～5 C that is selected from the substituting group replacement of A group
6～14Aryl, the heteroaryl that can be replaced by 1～5 substituting group that is selected from A group, the nitrogenous saturated heterocyclyl that can be replaced by 1～5 substituting group that is selected from the A group, the C that can be replaced by 1～5 substituting group that is selected from the A group
3～8Cycloalkyl or the C that can be replaced by 1～5 substituting group that is selected from A group
3～8Cycloalkenyl group,
B)-and NR-E-F, herein, E represents-CO-,-COO-,-CONR ' ,-SO
2NR '-or-SO
2-; F represents-Cyc or-can be selected from the C that following group replaces
1～6Alkyl, C
2～6Thiazolinyl or C
2～6Alkynyl :-halogen ,-NO
2,-CN ,-OR ,-O-C
1～6Alkylidene group-NRR ' ,-O-C
1～6Alkylidene group-OR ,-SR ,-SO
2-C
1～6Alkyl ,-SO-C
1～6Alkyl ,-COOR ,-COR ,-CO-C
6～14Aryl ,-CONRR ', SO
2NRR ' ,-NRCO-C
1～6Alkyl ,-NRR ' ,-NR '-C
1～6Alkylidene group-OR ,-NR "-C
1～6Alkylidene group-NRR ' and-Cyc and
C)-Z-R ' ,-Z-Cyc ,-Z-Alp-Cyc ,-Z-Alp-Z '-R ' or-Z-Alp-Z '-Cyc, herein, Z and Z ' can be identical also can be different, expression O, S or NR,
In the above-mentioned definition:
Nitrogenous saturated heterocyclyl be annular atoms comprise 1～2 N atom, also can contain the annular atoms of 1 O or S atom, also can have the nitrogenous saturated heterocyclyl of 5-7 unit of bridging, can condense with phenyl ring,
Heteroaryl is meant that containing 1-4 is selected from heteroatomic 5-6 unit's bicyclic heteroaryl of N, S, O or itself and phenyl ring and condenses the 2 ring type heteroaryls that form, and it can be a fractional saturation;
But except the following compound
(1) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidine also,
(2) 4-(4-morpholinyl)-2-phenylpyridine [2,3-d] pyrimidines-7 (1H)-ketone also,
(3) 4-(4-the morpholinyl)-pure and mild 6-methoxyl group-4-of 2-phenyl-6-quinazoline (4-morpholinyl)-2-phenylquinazoline,
(4) B is the R that phenyl ring, n are 2 or 3, exist
1All be-OMe and R
4bFor not replacing or be selected from the compound of the phenyl of 1～3 following substituting group replacement :-halogen ,-NO
2,-C
1～6Alkyl ,-O-C
1～6Alkyl ,-halo C
1～6Alkyl and-CONRaRc,
(5) B is the compound of imidazole ring,
(6) B is pyridine ring and R
4bBe the compound of unsubstituted phenyl,
(7) B is pyrazine ring and R
4bBe the compound of unsubstituted phenyl,
(8) B represents that phenyl ring, n are 1, R
1Expression-OH, R
4bExpression unsubstituted phenyl and R
2And R
3Be connected to the compound of piperidino-(1-position only) or 4-methyl isophthalic acid-piperazinyl with adjacent N atom,
(9) B represents phenyl ring, R
4bExpression 2-chloro-phenyl-and R
2And R
3Be connected to the compound of 1-piperazinyl with adjacent N atom,
(10) 4-(4-morpholinyl)-2-phenyl thieno-[2,3-d] pyrimidine and
(11) B represents that thiphene ring, n are O and R
2And R
3Be connected to the compound of 1-piperazinyl with adjacent N atom.
2. condensed heteroaryl derivatives as claimed in claim 1 or its salt is characterized in that R
2And R
3Formed NR
2R
3For-morpholino.
3. condensed heteroaryl derivatives as claimed in claim 2 or its salt is characterized in that, described R
1For-C
1～6Alkyl ,-C
2～6Thiazolinyl ,-C
2～6Alkynyl ,-C
3～8Cycloalkyl ,-can have 1～5 substituent C that is selected from the A group
6～14Aryl ,-can have 1～5 be selected from A organize substituent heteroaryl ,-halogen ,-NO
2,-CN ,-halo C
1～6Alkyl ,-ORb ,-SRb ,-SO
2-Rb ,-SO-Rb ,-COORb ,-CO-Rb ,-CONRaRb ,-SO
2NRaRb ,-NRaRb ,-NRa-CORb ,-NRa-SO
2Rb ,-O-CO-NRaRb or-NRaCO-COORb, the heteroaryl in the above-mentioned definition is meant that containing 1-4 is selected from heteroatomic 5-6 unit's bicyclic heteroaryl of N, S, O or itself and phenyl ring and condenses the 2 ring type heteroaryls that form, it can be a fractional saturation.
4. condensed heteroaryl derivatives as claimed in claim 3 or its salt is characterized in that, described B is a phenyl ring, and n is 1 or 2, R
1For-halogen ,-NO
2,-CN ,-halo C
1～6Alkyl ,-ORb ,-SRb ,-NRaRb ,-NRa-CORb or-NRa-SO
2Rb.
5. condensed heteroaryl derivatives as claimed in claim 1 or its salt is characterized in that, described B is pyridine, pyrazine or thiphene ring.
6. condensed heteroaryl derivatives as claimed in claim 5 or its salt is characterized in that, described R
4bFor can be selected from-OH ,-CH
2OH and-CONH
2The phenyl that replaces of at least one substituting group.
7. condensed heteroaryl derivatives as claimed in claim 1 or its salt is characterized in that it is selected from: N-[2-(3-benzene sulfonamido phenyl)-4-morpholino (6-quinazolyl)] ethanamide; 3-(4-morpholino pyrido [4,3-d] (2-pyrimidyl)) phenol; 3-(4-morpholino pyrido [3,2-d] (2-pyrimidyl) phenol; 3-(4-morpholino pyrido [3,4-d] (2-pyrimidyl) phenol; 3-(6-methoxyl group-4-morpholino (2-quinazolyl)) phenol; 3-(4-morpholino thieno-[3,2-d] (2-pyrimidyl)) phenol; And 3-(4-morpholino (2-pteridyl) phenol.
8. medical composition, it comprises the carrier that allows on the described condensed heteroaryl derivatives of claim 1 or its salt and the pharmacopedics.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000128472 | 2000-04-27 | ||
| JP2000128472 | 2000-04-27 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB018086543A Division CN1186324C (en) | 2000-04-27 | 2001-04-26 | Condensed heteroaryl derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1629145A CN1629145A (en) | 2005-06-22 |
| CN100345830C true CN100345830C (en) | 2007-10-31 |
Family
ID=18637911
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2004100557609A Expired - Lifetime CN100345830C (en) | 2000-04-27 | 2001-04-26 | Condensed heteroaryl derivatives |
| CNB018086543A Expired - Lifetime CN1186324C (en) | 2000-04-27 | 2001-04-26 | Condensed heteroaryl derivatives |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB018086543A Expired - Lifetime CN1186324C (en) | 2000-04-27 | 2001-04-26 | Condensed heteroaryl derivatives |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1277738B1 (en) |
| JP (1) | JP3649395B2 (en) |
| KR (1) | KR100774855B1 (en) |
| CN (2) | CN100345830C (en) |
| AT (1) | ATE503743T1 (en) |
| AU (1) | AU5261001A (en) |
| CA (1) | CA2407593C (en) |
| DE (1) | DE60144322D1 (en) |
| ES (1) | ES2360933T3 (en) |
| WO (1) | WO2001083456A1 (en) |
Families Citing this family (185)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003048152A2 (en) * | 2001-12-05 | 2003-06-12 | Tularik Inc. | Inflammation modulators |
| US7071190B2 (en) | 2002-02-15 | 2006-07-04 | Rigel Pharmaceuticals, Inc. | Inhibitors to tubulin polymerization |
| DK1513516T3 (en) * | 2002-06-06 | 2009-10-19 | Boehringer Ingelheim Pharma | Substituted 3-amino-thieno (2,3-b) -pyridine-2-carboxylic acid amide compounds and methods of preparation and their uses |
| ES2234439B2 (en) * | 2002-08-07 | 2006-11-01 | Universidade De Santiago De Compostela | PIRIDOTIENOTRIAZINAS REPLACED BY GENERAL FORMULA I AS ANTIPROTOZOARS FOR AQUACULTURE AND PREPARATION PROCEDURE. |
| WO2004017950A2 (en) * | 2002-08-22 | 2004-03-04 | Piramed Limited | Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents |
| ES2367141T3 (en) * | 2002-09-30 | 2011-10-28 | Bayer Pharma Aktiengesellschaft | CONDENSED AZOL-PYRIMIDINE DERIVATIVES. |
| AU2003258662A1 (en) * | 2002-10-02 | 2004-04-23 | Merck Patent Gmbh | Use of 4-amino-quinazolines as anti cancer agents |
| PT2316831E (en) * | 2002-11-21 | 2013-06-06 | Novartis Ag | 2-(morpholin-4-yl)pyrimidines as phosphotidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer |
| AU2003280188A1 (en) | 2002-12-06 | 2004-06-30 | Warner-Lambert Company Llc | Benzoxazin-3-ones and derivatives thereof as inhibitors of pi3k |
| JP2006512357A (en) * | 2002-12-20 | 2006-04-13 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | Benzoxazine and its derivatives as inhibitors of PI3K |
| JP2005104838A (en) | 2003-01-09 | 2005-04-21 | Tanabe Seiyaku Co Ltd | Condensed furan compound |
| CL2004000409A1 (en) | 2003-03-03 | 2005-01-07 | Vertex Pharma | COMPOUNDS DERIVED FROM 2- (REPLACED CILO) -1- (AMINO OR REPLACED OXI) -CHINAZOLINE, INHIBITORS OF IONIC SODIUM AND CALCIUM VOLTAGE DEPENDENTS; PHARMACEUTICAL COMPOSITION; AND USE OF THE COMPOUND IN THE TREATMENT OF ACUTE PAIN, CHRONIC, NEU |
| US7713983B2 (en) | 2003-03-03 | 2010-05-11 | Vertex Pharmaceuticals Incorporated | Quinazolines useful as modulators of ion channels |
| WO2004092196A2 (en) * | 2003-04-09 | 2004-10-28 | Exelixis, Inc. | Tie-2 modulators and methods of use |
| GB0313766D0 (en) * | 2003-06-13 | 2003-07-23 | Xenova Ltd | Pharmaceutical compounds |
| US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
| JP2007510745A (en) * | 2003-11-10 | 2007-04-26 | シンタ ファーマシューティカルズ コーポレーション | Fused heterocyclic compounds |
| BRPI0510560A (en) * | 2004-05-04 | 2007-11-20 | Warner Lambert Co | substituted pyrido [2,3-d] pyrimidin-7-ones and their derivatives as therapeutic agents |
| GB0415365D0 (en) * | 2004-07-09 | 2004-08-11 | Astrazeneca Ab | Pyrimidine derivatives |
| GB0415367D0 (en) * | 2004-07-09 | 2004-08-11 | Astrazeneca Ab | Pyrimidine derivatives |
| GB0415364D0 (en) * | 2004-07-09 | 2004-08-11 | Astrazeneca Ab | Pyrimidine derivatives |
| NZ552751A (en) | 2004-07-16 | 2010-11-26 | Sunesis Pharmaceuticals Inc | Thienopyrimidines useful as aurora kinase inhibitors |
| ES2341559T3 (en) * | 2004-07-23 | 2010-06-22 | The Medicines Company (Leipzig) Gmbh | PIRIDO (3 ', 2': 4,5) HAVING (3,2-D) PYRIMIDINES AND PIRIDO (3 ', 2': 4,5) FURO (3,2-D) PIRIMIDINES REPLACED FOR USE AS INHIBITORS OF THE RELEASE OF PDA-4 AND / OR TNF-ALFA. |
| EP1619197A1 (en) * | 2004-07-23 | 2006-01-25 | Curacyte Discovery GmbH | Substituted Pyrido[3',2':4,5]thieno[3,2-d]pyrimidin-2,4(1H,3H)diones and -4(3H)ones as well as Pyrido[3',2':4,5]furo[3,2-d]-pyrimidin-2,4(1H,3H)diones und -4(3H)ones as inhibitors of TNF-alpha release |
| WO2006010568A2 (en) * | 2004-07-23 | 2006-02-02 | Curacyte Discovery Gmbh | Substituted pyrido[3',2':4,5]thieno[3,2-d]pyrimidine-2,4(1 h,3h)-diones and -4(3h)-ones, pyrido[3',2':4,5]furo[3,2-d]pyrimidine-2,4(1 h,3h)-diones and -4(3h)-ones, and use thereof as inhibitors of tnf-alpha release |
| EP1619196A1 (en) * | 2004-07-23 | 2006-01-25 | Curacyte Discovery GmbH | Substituted Pyrido[3',2':4,5]thieno[3,2-d]pyrimidines and Pyrido[3',2':4,5]furo[3,2-d]-pyrimidines for use as inhibitors of PDA-4 and/or TNF-alpha release |
| US7928107B2 (en) | 2004-09-02 | 2011-04-19 | Vertex Pharmaceuticals Incorporated | Quinazolines useful as modulators of ion channels |
| JP2008513386A (en) * | 2004-09-20 | 2008-05-01 | ４エスシー アーゲー | Novel heterocyclic NF-κB inhibitor |
| CA2583259C (en) | 2004-10-08 | 2011-08-02 | Astellas Pharma Inc. | Aromatic ring fused pyrimidine derivative |
| CA2584507C (en) | 2004-10-20 | 2016-04-26 | Resverlogix Corp. | Flavanoids and isoflavanoids for the prevention and treatment of cardiovascular diseases |
| GB0423653D0 (en) * | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| AU2005302448B2 (en) | 2004-10-29 | 2012-07-19 | Biocryst Pharmaceuticals, Inc. | Therapeutic furopyrimidines and thienopyrimidines |
| US7875627B2 (en) | 2004-12-07 | 2011-01-25 | Abbott Laboratories | Thienopyridyl compounds that inhibit vanilloid receptor subtype 1 (VR1) and uses thereof |
| GB0428475D0 (en) * | 2004-12-30 | 2005-02-02 | 4 Aza Bioscience Nv | Pyrido(3,2-D)pyrimidine derivatives and pharmaceutical compositions useful as medicines for the treatment of autoimmune disorders |
| WO2006081659A1 (en) * | 2005-02-01 | 2006-08-10 | The University Of British Columbia | Meroterpenoid inhibitors of phosphoinositide 3 kinase (pi3k) |
| GB0508471D0 (en) * | 2005-04-26 | 2005-06-01 | Celltech R&D Ltd | Therapeutic agents |
| US8232278B2 (en) | 2005-06-24 | 2012-07-31 | Gilead Sciences, Inc. | Pyrido(3,2-D)pyrimidines and pharmaceutical compositions useful for treating hepatitis C |
| TW200740820A (en) | 2005-07-05 | 2007-11-01 | Takeda Pharmaceuticals Co | Fused heterocyclic derivatives and use thereof |
| ES2281251B1 (en) * | 2005-07-27 | 2008-08-16 | Laboratorios Almirall S.A. | NEW DERIVATIVES OF PIRIDO (3 ', 2': 4,5) FURO (3,2-D) PYRIMIDINE. |
| JP5368792B2 (en) | 2005-07-29 | 2013-12-18 | レスバーロジックス コーポレイション | Pharmaceutical compositions for the prevention and treatment of complex diseases and their delivery by insertable medical devices |
| EP1937279A2 (en) * | 2005-08-26 | 2008-07-02 | Novartis AG | Use of inhibitors of pi3k-c2a for the treatment of apoptosis-related disorders |
| EP1917252B1 (en) * | 2005-08-26 | 2014-01-01 | Merck Serono SA | Pyrazine derivatives and use as pi3k inhibitors |
| EP2322523B1 (en) | 2005-10-07 | 2019-01-02 | Exelixis, Inc. | Process for the preparation of Pyridopyrimidinone Inhibitors of PI3Kalpha |
| AU2006302148B2 (en) * | 2005-10-07 | 2012-12-06 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of PI3Kalpha |
| GB2431156A (en) * | 2005-10-11 | 2007-04-18 | Piramed Ltd | 1-cyclyl-3-substituted- -benzenes and -azines as inhibitors of phosphatidylinositol 3-kinase |
| EP1954699B1 (en) * | 2005-11-22 | 2012-09-19 | Kudos Pharmaceuticals Ltd | PYRIDO-, PYRAZO- AND PYRIMIDOPYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
| CN101360746B (en) * | 2005-11-22 | 2013-12-11 | 库多斯药物有限公司 | Pyrido-,pyrazo- and pyrimido-pyrimidine derivatives as mTOR inhibitors |
| GB0525081D0 (en) * | 2005-12-09 | 2006-01-18 | Astrazeneca Ab | Pyrimidine derivatives |
| EP1979325A1 (en) * | 2006-01-11 | 2008-10-15 | AstraZeneca AB | Morpholino pyrimidine derivatives and their use in therapy |
| JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | PI-3 Kinase inhibitors and methods of their use |
| NZ546477A (en) * | 2006-04-07 | 2009-04-30 | Auckland Uniservices Ltd | 4-Alkylamino-2-(heterocyclic)quinazolines and their use in cancer therapy |
| PL2024372T3 (en) | 2006-04-26 | 2010-11-30 | Hoffmann La Roche | Thieno[3,2-d]pyrimidine derivative useful as pi3k inhibitor |
| WO2007122410A1 (en) * | 2006-04-26 | 2007-11-01 | F.Hoffmann-La Roche Ag | Pyrimidine derivatives as pi3k inhibitors |
| CL2007001165A1 (en) | 2006-04-26 | 2008-01-25 | Hoffmann La Roche | 2- (1h-indazol-4-yl) -6- (4-methanesulfonyl-piperazin-1-ylmethyl) -4-morpholin-4-yl-thieno [3,2-d] pyrimidine; preparation procedure; pharmaceutical composition; process of preparing said composition; pharmaceutical kit; and use to treat diseases such as cancer, immune disorders and cardiovascular diseases. |
| KR101422301B1 (en) * | 2006-04-26 | 2014-07-30 | 에프. 호프만-라 로슈 아게 | Pharmaceutical compounds |
| TW200801012A (en) * | 2006-04-26 | 2008-01-01 | Piramed Ltd | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| GB0608820D0 (en) | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| US7592353B2 (en) | 2006-06-06 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Substituted 3-amino-thieno[2,3-b]pyridine-2-carboxylic acid amide compounds and processes for preparing and their uses |
| MX2008015908A (en) | 2006-06-12 | 2009-01-28 | Vertex Pharma | Thienopyrimidines useful as modulators of ion channels. |
| US8338435B2 (en) | 2006-07-20 | 2012-12-25 | Gilead Sciences, Inc. | Substituted pyrido(3,2-D) pyrimidines and pharmaceutical compositions for treating viral infections |
| MX2009001946A (en) | 2006-08-23 | 2009-03-05 | Kudos Pharm Ltd | 2-methylmorpholine pyrido-, pyrazo- and pyrimido-pyrimidine derivatives as mtor inhibitors. |
| CN101558067B (en) * | 2006-08-23 | 2014-05-28 | 库多斯药物有限公司 | 2-methylmorpholine pyrido-, pyrazo- and pyrimido-pyrimidine derivatives as mtor inhibitors |
| MX2009002046A (en) * | 2006-08-24 | 2009-03-06 | Astrazeneca Ab | Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders. |
| JP2010501537A (en) * | 2006-08-24 | 2010-01-21 | アストラゼネカ アクチボラグ | Morpholinopyrimidine derivatives useful for the treatment of proliferative disorders |
| RS51927B (en) | 2006-09-15 | 2012-02-29 | Pfizer Products Inc. | Pyrido (2,3-d)pyrimidinone compounds and their use as p13 inhibitors |
| US20100216820A1 (en) * | 2006-11-13 | 2010-08-26 | White Stephen L | Thienopyrimidiones for treatment of inflammatory disorders and cancers |
| US7888352B2 (en) | 2006-12-07 | 2011-02-15 | Piramed Limited | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| CN101675053B (en) | 2006-12-07 | 2014-03-12 | 健泰科生物技术公司 | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| WO2008075007A1 (en) * | 2006-12-21 | 2008-06-26 | Cancer Research Technology Limited | Morpholino-substituted bicycloheteroaryl compounds and their use as anti cancer agents |
| WO2008077649A1 (en) | 2006-12-26 | 2008-07-03 | Gilead Sciences, Inc. | Pyrido(3,2-d)pyrimidines useful for treating viral infectons |
| TW200840584A (en) | 2006-12-26 | 2008-10-16 | Gilead Sciences Inc | Pyrido(3,2-d)pyrimidines useful for treating viral infections |
| US8637531B2 (en) | 2006-12-26 | 2014-01-28 | Gilead Sciences, Inc. | Pyrido(3,2-d)pyridmidines useful for treating viral infections |
| PL2118074T3 (en) | 2007-02-01 | 2014-06-30 | Resverlogix Corp | Compounds for the prevention and treatment of cardiovascular diseases |
| AU2008213808B2 (en) | 2007-02-06 | 2011-11-10 | Novartis Ag | PI 3-kinase inhibitors and methods of their use |
| US20080233127A1 (en) * | 2007-03-21 | 2008-09-25 | Wyeth | Imidazolopyrimidine analogs and their use as pi3 kinase and mtor inhibitors |
| JP2010523639A (en) * | 2007-04-12 | 2010-07-15 | エフ．ホフマン−ラ ロシュ アーゲー | Pharmaceutical compounds |
| GB0707087D0 (en) | 2007-04-12 | 2007-05-23 | Piramed Ltd | Pharmaceutical compounds |
| PE20090717A1 (en) * | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS |
| WO2008152394A1 (en) * | 2007-06-12 | 2008-12-18 | F.Hoffmann-La Roche Ag | Pharmaceutical compounds |
| BRPI0814688A2 (en) | 2007-07-09 | 2017-06-06 | Astrazeneca Ab | compound, use of a compound, methods for producing an antiproliferative effect on a warm-blooded animal, and for treating disease, and, pharmaceutical composition |
| US20110009403A1 (en) * | 2007-10-05 | 2011-01-13 | S*Bio Pte Ltd. | 2-morpholinylpurines as inhibitors of pi3k |
| CN101889015B (en) * | 2007-10-05 | 2014-06-04 | 维拉斯通股份有限公司 | Pyrimidine substituted purine derivatives |
| AP2010005234A0 (en) | 2007-10-16 | 2010-04-30 | Wyeth Llc | Thienopyrimidine and pyrazolopyrimidline compoundsand their use as MTOR kinase and P13 kinase inhib itors |
| ES2537624T3 (en) * | 2007-10-26 | 2015-06-10 | F. Hoffmann-La Roche Ag | Purine derivatives useful as PI3 kinase inhibitors |
| GB0721095D0 (en) | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
| US20090149458A1 (en) * | 2007-11-27 | 2009-06-11 | Wyeth | PYRROLO[3,2-d]PYRIMIDINE COMPOUNDS AND THEIR USE AS PI3 KINASE AND mTOR KINASE INHIBITORS |
| AU2008343813B2 (en) * | 2007-12-19 | 2012-04-12 | Amgen Inc. | Inhibitors of PI3 kinase |
| EP2252296A1 (en) * | 2008-01-15 | 2010-11-24 | Wyeth LLC | 3h-[1,2,3]triazolo[4,5-d]pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
| US20090192176A1 (en) * | 2008-01-30 | 2009-07-30 | Wyeth | 1H-PYRAZOLO[3,4-D]PYRIMIDINE, PURINE, 7H-PURIN-8(9H)-ONE, 3H-[1,2,3]TRIAZOLO[4,5-D]PYRIMIDINE, AND THIENO[3,2-D]PYRIMIDINE COMPOUNDS, THEIR USE AS mTOR KINASE AND PI3 KINASE INHIBITORS, AND THEIR SYNTHESES |
| CL2009000241A1 (en) * | 2008-02-07 | 2010-09-03 | Chugai Pharmaceutical Co Ltd | Compounds derived from 5- (2-morpholin-4-yl-7h-pyrrolo [2,3-d] pyrimidin-4-yl) pyrimidin-2-ylamine; Preparation process; pharmaceutical composition; and use of the compounds to treat or prevent a proliferative disease such as cancer. |
| EP2279188B1 (en) | 2008-05-30 | 2015-01-28 | Genentech, Inc. | Purine pi3k inhibitor compounds and methods of use |
| BRPI0909957A2 (en) * | 2008-06-11 | 2016-04-19 | Genentech Inc | "compound, pharmaceutical composition, method of inhibiting abnormal cell growth or treating a hyperproliferative disorder in a mammal, method of treating cancer in a mammal" |
| CA2728183C (en) | 2008-06-20 | 2016-10-25 | Astrazeneca Ab | Compositions with and process for methylmorpholin-substituted pyrido [2,3-d] pryimidines |
| WO2009158404A1 (en) | 2008-06-26 | 2009-12-30 | Resverlogix Corp. | Methods of preparing quinazolinone derivatives |
| EP2310391A1 (en) * | 2008-06-27 | 2011-04-20 | S*BIO Pte Ltd | Pyrazine substituted purines |
| WO2010002954A1 (en) * | 2008-07-02 | 2010-01-07 | Wyeth | (2-aryl-7h-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
| PE20110403A1 (en) * | 2008-07-31 | 2011-07-04 | Genentech Inc | PYRIMIDINE FUSED BICYCLE COMPOUNDS IN THE TREATMENT OF CANCER |
| EP2350070A1 (en) | 2008-09-30 | 2011-08-03 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of pi3k and mtor |
| US20110257170A1 (en) * | 2008-10-03 | 2011-10-20 | Merck Serono Sa | 4-morpholino-pyrido[3,2-d]pyrimidines |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| WO2010045374A1 (en) * | 2008-10-15 | 2010-04-22 | Gilead Palo Alto, Inc. | 3-hydroquinazolin-4-one derivatives for use as stearoyl coa desaturase inhibitors |
| WO2010079431A2 (en) | 2009-01-08 | 2010-07-15 | Resverlogix Corp. | Compounds for the prevention and treatment of cardiovascular disease |
| EP2385832B1 (en) | 2009-01-08 | 2015-07-15 | Curis, Inc. | Phosphoinositide 3-kinase inhibitors with a zinc binding moiety |
| AU2010214095B2 (en) * | 2009-02-11 | 2015-12-24 | Merck Patent Gmbh | Novel amino azaheterocyclic carboxamides |
| ES2570456T3 (en) | 2009-02-12 | 2016-05-18 | Merck Serono Sa | 2-Morpholino-pyrido [3,2-d] pyrimidines |
| KR101709492B1 (en) | 2009-03-18 | 2017-02-23 | 리스버로직스 코퍼레이션 | Novel anti-inflammatory agents |
| CN105037364B (en) * | 2009-04-03 | 2018-04-27 | 维拉斯通股份有限公司 | The purine compound that pyrimidine as kinase inhibitor substitutes |
| DK2414362T3 (en) * | 2009-04-03 | 2014-09-22 | Verastem Inc | PYRIMIDINE-SUBSTITUTED PURINE COMPOUNDS AS KINASE INHIBITORS |
| WO2010120987A1 (en) * | 2009-04-17 | 2010-10-21 | Wyeth Llc | Ring fused, ureidoaryl- and carbamoylaryl-bridged morpholino-pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
| KR102215167B1 (en) | 2009-04-22 | 2021-02-16 | 리스버로직스 코퍼레이션 | Novel anti-inflammatory agents |
| UY32582A (en) | 2009-04-28 | 2010-11-30 | Amgen Inc | 3 KINASE PHOSPHINOSITI INHIBITORS AND / OR MAMMAL OBJECTIVE |
| CA2771594C (en) * | 2009-08-20 | 2018-05-01 | Karus Therapeutics Limited | Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors |
| KR101698631B1 (en) | 2009-09-03 | 2017-01-20 | 브리스톨-마이어스 스큅 컴퍼니 | Quinazolines as potassium ion channel inhibitors |
| CN102020657A (en) * | 2009-09-11 | 2011-04-20 | 上海艾力斯医药科技有限公司 | Condensed heteroaryl derivative, and preparation method and application thereof |
| CA2775204A1 (en) * | 2009-09-24 | 2011-03-31 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Fused imidazo [3, 2 - d] pyraz ines as pi3 kinase inhibitors |
| GB0918249D0 (en) | 2009-10-19 | 2009-12-02 | Respivert Ltd | Compounds |
| MX2012005225A (en) | 2009-11-12 | 2012-07-25 | Hoffmann La Roche | N-7 substituted purine and pyrazolopyrimidine compounds, compositions and methods of use. |
| CN105859689A (en) * | 2009-12-28 | 2016-08-17 | 财团法人生物技术开发中心 | Novel pyrimidine compounds as mTOR and P13K inhibitors |
| AR079814A1 (en) * | 2009-12-31 | 2012-02-22 | Otsuka Pharma Co Ltd | HETEROCICLICAL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USES |
| EP2528606B1 (en) | 2010-01-28 | 2014-09-24 | Alexander Levitzki | Quinazoline-based t cell proliferation inhibitors |
| AR080151A1 (en) | 2010-02-09 | 2012-03-14 | Exelixis Inc | METHODS TO TREAT CANCER USING PI 3K PYRIDOPIRIMIDINONE INHIBITORS AND MTOR IN COMBINATION WITH AUTOPHAGIA INHIBITORS |
| JP5770751B2 (en) * | 2010-02-22 | 2015-08-26 | エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ | Pyrido [3,2-d] pyrimidine-based PI3K delta inhibitor compounds and methods of use |
| US8912184B1 (en) | 2010-03-01 | 2014-12-16 | Alzheimer's Institute Of America, Inc. | Therapeutic and diagnostic methods |
| US9090674B2 (en) * | 2010-05-17 | 2015-07-28 | The Board Of Regents Of The University Of Texas System | Rapid isolation of monoclonal antibodies from animals |
| CN102268014B (en) * | 2010-06-03 | 2015-06-03 | 上海艾力斯医药科技有限公司 | Condensed heteroaryl derivative and its preparation method and use |
| SA111320519B1 (en) | 2010-06-11 | 2014-07-02 | Astrazeneca Ab | Pyrimidinyl Compounds for Use as ATR Inhibitors |
| CA2802808A1 (en) | 2010-07-14 | 2012-01-19 | F. Hoffmann-La Roche Ag | Purine compounds selective for pi3k p110 delta, and methods of use |
| UA110113C2 (en) * | 2010-07-29 | 2015-11-25 | BICYCLIC AZAGETEROCYCLIC CARBOXAMIDES | |
| CN103140484B (en) * | 2010-07-29 | 2015-04-22 | 默克专利有限公司 | Cyclic amine azaheterocyclic carboxamides |
| EP2624695B1 (en) | 2010-10-08 | 2015-09-23 | Nivalis Therapeutics, Inc. | Novel substituted quinoline compounds as s-nitrosoglutathione reductase inhibitors |
| UY33337A (en) | 2010-10-18 | 2011-10-31 | Respivert Ltd | SUBSTITUTED DERIVATIVES OF 1H-PIRAZOL [3,4-d] PYRIMIDINE AS INHIBITORS OF PHOSFOINOSITIDE 3-KINASES |
| WO2012058671A1 (en) | 2010-10-31 | 2012-05-03 | Endo Pharmaceuticals Inc. | Substituted quinazoline and pyrido-pyrimidine derivatives |
| CN102558185B (en) * | 2010-12-09 | 2016-02-10 | 中国科学院上海药物研究所 | Pyrido pyrrole triazine compound, Preparation Method And The Use |
| KR101548439B1 (en) | 2010-12-16 | 2015-08-28 | 에프. 호프만-라 로슈 아게 | Tricyclic pi3k inhibitor compounds and methods of use |
| US9249132B2 (en) * | 2010-12-16 | 2016-02-02 | Nivalis Therapeutics, Inc. | Substituted bicyclic aromatic compounds as S-nitrosoglutathione reductase inhibitors |
| CA2827770A1 (en) * | 2011-02-25 | 2012-11-01 | Takeda Pharmaceutical Company Limited | N-substituted oxazinopteridines and oxazinopteridinones |
| WO2012131297A1 (en) | 2011-03-28 | 2012-10-04 | Jonathan Bayldon Baell | Pyrido [3',2' :4,5] thieno [3, 2-d] pyrimidin- 4 - ylamine derivatives and their therapeutical use |
| WO2012135571A1 (en) | 2011-04-01 | 2012-10-04 | Curis, Inc. | Phosphoinositide 3-kinase inhibitor with a zinc binding moiety |
| CN102731525A (en) * | 2011-04-08 | 2012-10-17 | 上海艾力斯医药科技有限公司 | Benzomorpholine derivative |
| KR101106778B1 (en) * | 2011-05-24 | 2012-01-18 | 한국바이오시스템(주) | Wastewater treatment apparatus for public facilities and apartment house by natural purification and wastewater treatment method and water circulation system using the wastewater treatment apparatus |
| GEP20166432B (en) | 2011-09-27 | 2016-02-10 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| HUE044986T2 (en) | 2011-11-01 | 2019-11-28 | Resverlogix Corp | Oral immediate release formulations for substituted quinazolinones |
| AU2012340869B2 (en) | 2011-11-23 | 2017-03-02 | Cancer Research Technology Limited | Thienopyrimidine inhibitors of atypical protein kinase C |
| UY34632A (en) | 2012-02-24 | 2013-05-31 | Novartis Ag | OXAZOLIDIN- 2- ONA COMPOUNDS AND USES OF THE SAME |
| GB201204125D0 (en) | 2012-03-08 | 2012-04-25 | Karus Therapeutics Ltd | Compounds |
| EA025465B1 (en) | 2012-03-13 | 2016-12-30 | Респайверт Лимитед | METHOD OF INCREASING THE STABILITY TO CHEMICAL DEGRADATION OF A PHARMACEUTICAL FORMULATION COMPRISING 6-(2-((4-AMINO-3-(3-HYDROXYPHENYL)-1H-PYRAZOLO[3,4-d]PYRIMIDIN-1-YL)METHYL)-3-(2-CHLOROBENZYL)-4-OXO-3,4-DIHYDROQYINAZOLIN-5-YL)-N,N-BIS(2-METHOXYETHYL)HEX-5-YNAMIDE |
| WO2014022728A1 (en) * | 2012-08-02 | 2014-02-06 | Endo Pharmaceuticals, Inc | Substituted 5 - (quinazolin - 2 - yl) pyrimidin- 2 -amine derivatives useful as pi3k/mtor inhibitors for the treatment of cancer |
| CN104797573A (en) | 2012-11-07 | 2015-07-22 | 卡鲁斯治疗有限公司 | Novel histone deacetylase inhibitors and their use in therapy |
| US9296733B2 (en) | 2012-11-12 | 2016-03-29 | Novartis Ag | Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases |
| US9073878B2 (en) | 2012-11-21 | 2015-07-07 | Zenith Epigenetics Corp. | Cyclic amines as bromodomain inhibitors |
| WO2014080291A2 (en) | 2012-11-21 | 2014-05-30 | Rvx Therapeutics Inc. | Biaryl derivatives as bromodomain inhibitors |
| CN105073744B (en) | 2012-12-21 | 2019-11-08 | 齐尼思表观遗传学有限公司 | Novel heterocyclic compounds as bromine structural domain inhibitor |
| AP2015008707A0 (en) | 2013-03-14 | 2015-09-30 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| JO3279B1 (en) | 2013-03-15 | 2018-09-16 | Respivert Ltd | 2-((4-amino-3-(3-fluoro-5-hydroxyphenyl)-1h-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-(2-(trifluoromethyl)benzyl)quinazolin-4(3h)-one derivatives and their use as phosphoinositide 3-kinase inhibitors |
| US9227977B2 (en) | 2013-03-15 | 2016-01-05 | Respivert Ltd. | Phosphoinositide 3-kinase inhibitors |
| WO2014181137A1 (en) | 2013-05-10 | 2014-11-13 | Karus Therapeutics Ltd | Novel histone deacetylase inhibitors |
| AU2014336775B2 (en) * | 2013-10-16 | 2018-04-05 | Shanghai Yingli Pharmaceutical Co., Ltd | Fused heterocyclic compound, preparation method therefor, pharmaceutical composition, and uses thereof |
| CN103664876B (en) * | 2013-11-01 | 2016-04-20 | 苏州东南药业股份有限公司 | Quinoline derivatives and uses thereof |
| GB201402431D0 (en) | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| CN104311494A (en) * | 2014-10-16 | 2015-01-28 | 西安交通大学 | m-(4-morpholinyl-2-quinazolinyl) benzamide compounds and synthetic method and application thereof |
| GB201419228D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| GB201419264D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| US10111885B2 (en) | 2015-03-13 | 2018-10-30 | Resverlogix Corp. | Compositions and therapeutic methods for the treatment of complement-associated diseases |
| KR101845931B1 (en) | 2015-06-18 | 2018-04-05 | 한국화학연구원 | Heteroaryl derivatives or pharmaceutically acceptable salts thereof, preparation method thereof and pharmaceutical composition for use in preventing or treating PI3 kinase related diseases |
| GB201514751D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514754D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514758D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Formulation |
| GB201514760D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds and method of use |
| CN105153190B (en) * | 2015-08-21 | 2017-07-21 | 江西科技师范大学 | Heterocycle miazines compound of the amide structure containing biaryl and its preparation method and application |
| US10399946B2 (en) | 2015-09-10 | 2019-09-03 | Laurel Therapeutics Ltd. | Solid forms of an S-Nitrosoglutathione reductase inhibitor |
| US10696688B2 (en) | 2015-11-23 | 2020-06-30 | Council Of Scientific & Industrial Research | Fused pyrimidines as isoform selective phosphoinositide-3-kinase-alpha inhibitors and process for preparation thereof |
| EP3394056B1 (en) | 2015-12-22 | 2021-04-14 | Shy Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
| WO2017184547A1 (en) | 2016-04-18 | 2017-10-26 | New York University | Quinoline compounds as modulators of rage activity and uses thereof |
| EP4331679A3 (en) | 2017-06-21 | 2024-04-03 | Shy Therapeutics LLC | Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease |
| CN109384782A (en) | 2017-08-04 | 2019-02-26 | 厦门大学 | Substituted five-membered and hexa-member heterocycle class compound, preparation method, pharmaceutical composition and application thereof |
| CN107805255B (en) * | 2017-09-22 | 2020-06-16 | 中国药科大学 | Furan [3, 2-b ] pyridine-2 (1H) -ketone compound, preparation method and medical application |
| KR20190043437A (en) | 2017-10-18 | 2019-04-26 | 씨제이헬스케어 주식회사 | Heterocylic compound as a protein kinase inhibitor |
| CA3102326A1 (en) | 2018-07-26 | 2020-01-30 | Domain Therapeutics | Substituted quinazolinone derivatives and their use as positive allosteric modulators of mglur4 |
| WO2020055840A1 (en) | 2018-09-11 | 2020-03-19 | Curis Inc. | Combination therapy with a phosphoinositide 3-kinase inhibitor with a zinc binding moiety |
| CN110950868B (en) * | 2018-09-27 | 2022-05-13 | 苏州锐明新药研发有限公司 | Pyrazolopyrimidine compound, preparation method thereof and application of pyrazolopyrimidine compound in preparation of anti-cancer drugs |
| CN109796415B (en) * | 2019-03-29 | 2020-10-30 | 武汉德诺美生物医药股份有限公司 | EGFR inhibitor and application thereof |
| KR102338609B1 (en) | 2019-05-20 | 2021-12-14 | 보령제약 주식회사 | Pyrido-pyrimidin compound and pharmaceutical composition for use in preventing or treating PI3 kinase related diseases |
| WO2021113633A1 (en) * | 2019-12-05 | 2021-06-10 | Verge Analytics, Inc. | Fused tricyclic heterocyclic compounds as inhibitors of pikfyve kinase useful for the treatment of neurological diseases |
| CN113072543B (en) * | 2020-01-03 | 2022-07-22 | 南方医科大学 | 2-aromatic heterocyclic quinazoline ketone compound and preparation method and application thereof |
| TW202237095A (en) * | 2020-12-03 | 2022-10-01 | 德商艾斯巴赫生物有限公司 | Alc1 inhibitors and synergy with parpi |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3808211A (en) * | 1972-06-12 | 1974-04-30 | Morton Norwich Products Inc | 4-(substituted amino)-2-(5-nitro-2-furyl)pyrimido(4,5-d)pyrimidines |
| JPS58172379A (en) * | 1982-04-02 | 1983-10-11 | Showa Denko Kk | Novel quinazoline derivative |
| CN1112365A (en) * | 1993-06-17 | 1995-11-22 | 株式会社大塚制药工场 | Phosphonic diester derivative |
| GB2295387A (en) * | 1994-11-23 | 1996-05-29 | Glaxo Inc | Quinazoline antagonists of alpha 1c adrenergic receptors |
| JPH1087492A (en) * | 1996-06-25 | 1998-04-07 | Ono Pharmaceut Co Ltd | Nitrogen monoxide production inhibitor |
| JPH10175977A (en) * | 1996-12-13 | 1998-06-30 | Takeda Chem Ind Ltd | Condensed indole derivative, its production and use thereof |
| CN1208404A (en) * | 1996-10-01 | 1999-02-17 | 协和发酵工业株式会社 | Nitrogenous heterocyclic compounds |
| JPH11209287A (en) * | 1998-01-23 | 1999-08-03 | Ono Pharmaceut Co Ltd | Inhibitor of nitrogen monoxide production |
| WO1999051582A1 (en) * | 1998-03-31 | 1999-10-14 | Kyowa Hakko Kogyo Co., Ltd. | Nitrogenous heterocyclic compounds |
| US5990117A (en) * | 1998-04-15 | 1999-11-23 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to quinazoline derivatives |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH612432A5 (en) | 1975-05-12 | 1979-07-31 | Sandoz Ag | |
| JPS56120768A (en) | 1980-01-31 | 1981-09-22 | Ciba Geigy Ag | Color developing quinazoline compound |
| US4560692A (en) | 1984-07-18 | 1985-12-24 | Hoffmann-La Roche Inc. | 4-Piperidino-2-phenylquinolines |
| JPH02129169A (en) | 1988-11-08 | 1990-05-17 | Ube Ind Ltd | Quinoline compound and pharmaceutical use thereof |
| US5304554A (en) | 1990-04-27 | 1994-04-19 | Emory University | 4-[(alkyl or dialkyl)amino]quinolines and their method of preparation |
-
2001
- 2001-04-26 CA CA2407593A patent/CA2407593C/en not_active Expired - Lifetime
- 2001-04-26 AT AT01925981T patent/ATE503743T1/en not_active IP Right Cessation
- 2001-04-26 WO PCT/JP2001/003650 patent/WO2001083456A1/en active Application Filing
- 2001-04-26 CN CNB2004100557609A patent/CN100345830C/en not_active Expired - Lifetime
- 2001-04-26 JP JP2001580885A patent/JP3649395B2/en not_active Expired - Lifetime
- 2001-04-26 CN CNB018086543A patent/CN1186324C/en not_active Expired - Lifetime
- 2001-04-26 DE DE60144322T patent/DE60144322D1/en not_active Expired - Lifetime
- 2001-04-26 EP EP01925981A patent/EP1277738B1/en not_active Expired - Lifetime
- 2001-04-26 KR KR1020027014412A patent/KR100774855B1/en active IP Right Grant
- 2001-04-26 ES ES01925981T patent/ES2360933T3/en not_active Expired - Lifetime
- 2001-04-26 AU AU52610/01A patent/AU5261001A/en not_active Abandoned
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3808211A (en) * | 1972-06-12 | 1974-04-30 | Morton Norwich Products Inc | 4-(substituted amino)-2-(5-nitro-2-furyl)pyrimido(4,5-d)pyrimidines |
| JPS58172379A (en) * | 1982-04-02 | 1983-10-11 | Showa Denko Kk | Novel quinazoline derivative |
| CN1112365A (en) * | 1993-06-17 | 1995-11-22 | 株式会社大塚制药工场 | Phosphonic diester derivative |
| GB2295387A (en) * | 1994-11-23 | 1996-05-29 | Glaxo Inc | Quinazoline antagonists of alpha 1c adrenergic receptors |
| JPH1087492A (en) * | 1996-06-25 | 1998-04-07 | Ono Pharmaceut Co Ltd | Nitrogen monoxide production inhibitor |
| CN1208404A (en) * | 1996-10-01 | 1999-02-17 | 协和发酵工业株式会社 | Nitrogenous heterocyclic compounds |
| JPH10175977A (en) * | 1996-12-13 | 1998-06-30 | Takeda Chem Ind Ltd | Condensed indole derivative, its production and use thereof |
| JPH11209287A (en) * | 1998-01-23 | 1999-08-03 | Ono Pharmaceut Co Ltd | Inhibitor of nitrogen monoxide production |
| WO1999051582A1 (en) * | 1998-03-31 | 1999-10-14 | Kyowa Hakko Kogyo Co., Ltd. | Nitrogenous heterocyclic compounds |
| US5990117A (en) * | 1998-04-15 | 1999-11-23 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to quinazoline derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60144322D1 (en) | 2011-05-12 |
| CN1426398A (en) | 2003-06-25 |
| EP1277738A1 (en) | 2003-01-22 |
| JP3649395B2 (en) | 2005-05-18 |
| WO2001083456A1 (en) | 2001-11-08 |
| KR20020093086A (en) | 2002-12-12 |
| ES2360933T3 (en) | 2011-06-10 |
| CA2407593C (en) | 2011-01-11 |
| CA2407593A1 (en) | 2001-11-08 |
| CN1629145A (en) | 2005-06-22 |
| CN1186324C (en) | 2005-01-26 |
| AU5261001A (en) | 2001-11-12 |
| EP1277738A4 (en) | 2005-02-09 |
| EP1277738B1 (en) | 2011-03-30 |
| ATE503743T1 (en) | 2011-04-15 |
| KR100774855B1 (en) | 2007-11-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100345830C (en) | Condensed heteroaryl derivatives | |
| CN1173975C (en) | Imidazopyridine derivatives | |
| CN1294135C (en) | Pyrrolopyrimidines as protein kinase inhitibors | |
| CN1211373C (en) | 2,4-di (hetero-) arylamino (-oxy)-5-substituted pyrimidines as antineoplastic agents | |
| CN1233188A (en) | Medicines comprising Rho kinase inhibitor | |
| CN1038511C (en) | Imidazopyridine | |
| CN1551881A (en) | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions | |
| CN1993129A (en) | Thienopyrimidines and thiazolopyrimidines for use in medicine | |
| CN1906190A (en) | Selective kinase inhibitors | |
| CN1441783A (en) | Medicine comprising dicyanopyridine derivative | |
| CN1701074A (en) | Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors | |
| CN1656073A (en) | Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases | |
| CN1642915A (en) | Benzamide derivatives useful as histone deacetylase inhibitors | |
| CN101039914A (en) | Trifluoromethyl substituted benzamide as kinase inhibitors | |
| CN1055182A (en) | N-(pyrrolo-" 2,3-d " pyrimidin-3-yl acyl group)-glutamic acid derivatives | |
| CN1856480A (en) | P-38 kinase inhibitors | |
| CN1849325A (en) | Thiazolo-, oxazalo and imidazolo-quinazoline compounds capable of inhibiting prot ein kinases | |
| CN1694886A (en) | Novel imidazopyrazines as cyclin dependent kinase inhibitors | |
| CN1694704A (en) | Use of (1H-benzimidazole-2-yl)-(piperazineyl)- ketaderavitive and correlative compound used as histamine H4 receptor antagonist for the treatment of allergy and asthma | |
| CN101031565A (en) | Substituted 2h-1,3-benzoxazin-4(3h)-ones | |
| CN101031560A (en) | Cyclic diaryl ureas suitable as tyrosine kinase inhibitors | |
| CN1726216A (en) | C-6 modified indazolylpyrrolotriazines | |
| CN1809565A (en) | Pyrrolodihydroisoquinolines as pde10 inhibitors | |
| CN1761671A (en) | 4-aminothieno [2,3-d] pyrimidine-6-carbonitrile derivatives as PDE7 inhibitors | |
| CN101052634A (en) | Anthranilamide pyridinureas as vegf receptor kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term |
Granted publication date: 20071031 |
|
| CX01 | Expiry of patent term |